11-111781170-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781170
    reference: chr 11
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.205C>A
  hgvsp: ENSP00000432182.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.4C>A
  hgvsp: ENSP00000435960.1:p.Arg2Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.205C>A
  hgvsp: ENSP00000227251.3:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.205C>A
  hgvsp: ENSP00000437149.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.205C>A
  hgvsp: ENSP00000434269.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.205C>A
  hgvsp: ENSP00000431754.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.4C>A
  hgvsp: ENSP00000434793.1:p.Arg2Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.205C>A
  hgvsp: ENSP00000436089.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.4C>A
  hgvsp: ENSP00000435046.1:p.Arg2Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.205C>A
  hgvsp: ENSP00000434247.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.205C>A
  hgvsp: ENSP00000436051.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.205C>A
  hgvsp: ENSP00000433560.1:p.Arg69Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.205C>A
  hgvsp: ENST00000533879.1:c.205C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.4C>A
  hgvsp: ENSP00000435411.1:p.Arg2Ser
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg69Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/11-111781184-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781184
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781184
    reference: chr 11
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-11G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-11G>T
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

11-111781189-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781189
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781189
    reference: chr 11
allele count: 17
allele frequency: 1.400629459357029e-4
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-16A>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-16A>G
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

11-111781198-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781198
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781198
    reference: chr 11
allele count: 92
allele frequency: 7.581001351395893e-4
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-25C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-25C>T
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 22127
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

11-111781207-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781207
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781206
    reference: chr 11
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-35delT
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: GA
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/11-111781209-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781209
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781209
    reference: chr 11
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-36T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-36T>G
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8672
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

11-111781211-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781211
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781211
    reference: chr 11
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-38C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-38C>A
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/11-111781212-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781212
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781212
    reference: chr 11
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-39T>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-39T>G
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-111781212-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781212
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781212
    reference: chr 11
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-39T>C
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-111781225-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111781225
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111781225
    reference: chr 11
allele count: 11
allele frequency: 9.068724442685661e-5
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434793
  ensembl transcript: ENST00000526167
  gene symbol: CRYAB
  hgvsc: ENST00000526167.1:c.1-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435960
  ensembl transcript: ENST00000528961
  gene symbol: CRYAB
  hgvsc: ENST00000528961.1:c.1-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435411
  ensembl transcript: ENST00000525823
  gene symbol: CRYAB
  hgvsc: ENST00000525823.1:c.-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.202-52A>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435046
  ensembl transcript: ENST00000533280
  gene symbol: CRYAB
  hgvsc: ENST00000533280.1:c.1-52A>C
  variant of: http://identifiers.org/hgnc/2389
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21846
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-111782199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782199
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782199
    reference: chr 11
allele count: 1
allele frequency: 2.067482633145882e-5
allele num: 48368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+49G>A
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25572
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5205
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4798
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3804
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-111782218-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782218
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782218
    reference: chr 11
allele count: 1
allele frequency: 1.925372559590281e-5
allele num: 51938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+30G>C
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5519
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ

11-111782218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782218
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782218
    reference: chr 11
allele count: 2
allele frequency: 3.850745119180561e-5
allele num: 51938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+30G>A
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11756
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4719
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

11-111782224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782224
    reference: chr 11
allele count: 2
allele frequency: 3.687043728338618e-5
allele num: 54244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+24G>A
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-111782225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782225
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782225
    reference: chr 11
allele count: 17
allele frequency: 3.074919509459899e-4
allele num: 55286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+23C>T
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28579
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10687
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-111782230-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782230
    reference: chr 11
allele count: 1
allele frequency: 1.705611461709023e-5
allele num: 58630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+18T>C
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3615
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3702
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

11-111782231-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782231
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782231
    reference: chr 11
allele count: 2
allele frequency: 3.378036009863865e-5
allele num: 59206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+17C>T
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28074
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11923
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-111782231-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782231
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782231
    reference: chr 11
allele count: 2
allele frequency: 3.378036009863865e-5
allele num: 59206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+17C>G
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-111782234-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782234
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782234
    reference: chr 11
allele count: 1
allele frequency: 1.624484226258163e-5
allele num: 61558
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.201+14C>G
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

11-111782261-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782261
    reference: chr 11
allele count: 1
allele frequency: 1.192264587357226e-5
allele num: 83874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.188C>A
  hgvsp: ENSP00000436051.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.188C>A
  hgvsp: ENSP00000436089.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.188C>A
  hgvsp: ENSP00000434269.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.188C>A
  hgvsp: ENSP00000431754.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.188C>A
  hgvsp: ENSP00000434247.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.188C>A
  hgvsp: ENSP00000435931.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.188C>A
  hgvsp: ENSP00000437149.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.188C>A
  hgvsp: ENSP00000227251.3:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.188C>A
  hgvsp: ENSP00000433560.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.188C>A
  hgvsp: ENSP00000432182.1:p.Thr63Asn
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23968
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr63Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

11-111782267-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782267
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782267
    reference: chr 11
allele count: 2
allele frequency: 2.27748929580031e-5
allele num: 87816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.182T>A
  hgvsp: ENSP00000434247.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.182T>A
  hgvsp: ENSP00000433560.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.182T>A
  hgvsp: ENSP00000435931.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.182T>A
  hgvsp: ENSP00000437149.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.182T>A
  hgvsp: ENSP00000434269.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.182T>A
  hgvsp: ENSP00000436051.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.182T>A
  hgvsp: ENSP00000436089.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.182T>A
  hgvsp: ENSP00000432182.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.182T>A
  hgvsp: ENSP00000431754.1:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.182T>A
  hgvsp: ENSP00000227251.3:p.Phe61Tyr
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2898
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe61Tyr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

11-111782275-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782275
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782275
    reference: chr 11
allele count: 4
allele frequency: 4.30070531567177e-5
allele num: 93008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.174C>A
  hgvsp: ENST00000529647.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.174C>A
  hgvsp: ENST00000527950.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.174C>A
  hgvsp: ENST00000531198.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.174C>A
  hgvsp: ENST00000227251.3:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.174C>A
  hgvsp: ENST00000526180.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.174C>A
  hgvsp: ENST00000528628.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.174C>A
  hgvsp: ENST00000533971.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.174C>A
  hgvsp: ENST00000533475.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.174C>A
  hgvsp: ENST00000527899.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.174C>A
  hgvsp: ENST00000533879.1:c.174C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28315
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro58Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

11-111782277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782277
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782277
    reference: chr 11
allele count: 1
allele frequency: 1.065734504220309e-5
allele num: 93832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.172C>T
  hgvsp: ENSP00000436089.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.172C>T
  hgvsp: ENSP00000434269.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.172C>T
  hgvsp: ENSP00000435931.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.172C>T
  hgvsp: ENSP00000433560.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.172C>T
  hgvsp: ENSP00000431754.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.172C>T
  hgvsp: ENSP00000436051.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.172C>T
  hgvsp: ENSP00000227251.3:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.172C>T
  hgvsp: ENSP00000432182.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.172C>T
  hgvsp: ENSP00000434247.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.172C>T
  hgvsp: ENSP00000437149.1:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro58Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

11-111782282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782282
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782282
    reference: chr 11
allele count: 1
allele frequency: 1.040193059831905e-5
allele num: 96136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.167G>A
  hgvsp: ENSP00000436051.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.167G>A
  hgvsp: ENSP00000434247.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.167G>A
  hgvsp: ENSP00000431754.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.167G>A
  hgvsp: ENSP00000436089.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.167G>A
  hgvsp: ENSP00000434269.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.167G>A
  hgvsp: ENSP00000437149.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.167G>A
  hgvsp: ENSP00000435931.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.167G>A
  hgvsp: ENSP00000432182.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.167G>A
  hgvsp: ENSP00000433560.1:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.167G>A
  hgvsp: ENSP00000227251.3:p.Arg56Gln
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29457
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg56Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

11-111782284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782284
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782284
    reference: chr 11
allele count: 1898
allele frequency: 1.934602682757777e-2
allele num: 98108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.165G>A
  hgvsp: ENST00000527950.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.165G>A
  hgvsp: ENST00000227251.3:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.165G>A
  hgvsp: ENST00000533879.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.165G>A
  hgvsp: ENST00000528628.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.165G>A
  hgvsp: ENST00000531198.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.165G>A
  hgvsp: ENST00000533475.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.165G>A
  hgvsp: ENST00000526180.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.165G>A
  hgvsp: ENST00000529647.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.165G>A
  hgvsp: ENST00000533971.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.165G>A
  hgvsp: ENST00000527899.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 1.75e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 3.25e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 1.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 29316
  bin: 2.25e1
  variant carriers: 327
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 3.75e1
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 2.75e1
  variant carriers: 284
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu55Leu
num of homozygotes: 31
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

11-111782297-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782297
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782297
    reference: chr 11
allele count: 45
allele frequency: 4.470405912856888e-4
allele num: 100662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.152C>T
  hgvsp: ENSP00000227251.3:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.152C>T
  hgvsp: ENSP00000435931.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.152C>T
  hgvsp: ENSP00000436051.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.152C>T
  hgvsp: ENSP00000434247.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.152C>T
  hgvsp: ENSP00000432182.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.152C>T
  hgvsp: ENSP00000434269.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.152C>T
  hgvsp: ENSP00000431754.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.152C>T
  hgvsp: ENSP00000437149.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.152C>T
  hgvsp: ENSP00000436089.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.152C>T
  hgvsp: ENSP00000433560.1:p.Pro51Leu
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29206
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8624
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11736
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro51Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-111782300-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782300
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782300
    reference: chr 11
allele count: 1
allele frequency: 9.910213465998057e-6
allele num: 100906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.149G>A
  hgvsp: ENSP00000435931.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.149G>A
  hgvsp: ENSP00000434247.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.149G>A
  hgvsp: ENSP00000432182.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.149G>A
  hgvsp: ENSP00000227251.3:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.149G>A
  hgvsp: ENSP00000434269.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.149G>A
  hgvsp: ENSP00000437149.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.149G>A
  hgvsp: ENSP00000431754.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.149G>A
  hgvsp: ENSP00000433560.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.149G>A
  hgvsp: ENSP00000436051.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.149G>A
  hgvsp: ENSP00000436089.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg50Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-111782317-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782317
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782317
    reference: chr 11
allele count: 1
allele frequency: 9.867187654174808e-6
allele num: 101346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.132G>A
  hgvsp: ENST00000527950.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.132G>A
  hgvsp: ENST00000526180.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.132G>A
  hgvsp: ENST00000527899.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.132G>A
  hgvsp: ENST00000227251.3:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.132G>A
  hgvsp: ENST00000529647.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.132G>A
  hgvsp: ENST00000533879.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.132G>A
  hgvsp: ENST00000533475.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.132G>A
  hgvsp: ENST00000533971.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.132G>A
  hgvsp: ENST00000528628.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.132G>A
  hgvsp: ENST00000531198.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu44Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-111782319-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782319
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782319
    reference: chr 11
allele count: 1
allele frequency: 9.88513473438643e-6
allele num: 101162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.130C>A
  hgvsp: ENSP00000431754.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.130C>A
  hgvsp: ENSP00000435931.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.130C>A
  hgvsp: ENSP00000436051.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.130C>A
  hgvsp: ENSP00000227251.3:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.130C>A
  hgvsp: ENSP00000434247.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.130C>A
  hgvsp: ENSP00000436089.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.130C>A
  hgvsp: ENSP00000434269.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.130C>A
  hgvsp: ENSP00000433560.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.130C>A
  hgvsp: ENSP00000437149.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.130C>A
  hgvsp: ENSP00000432182.1:p.Leu44Met
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9294
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu44Met
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-111782323-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782323
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782323
    reference: chr 11
allele count: 3
allele frequency: 2.990311391092859e-5
allele num: 100324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.126T>G
  hgvsp: ENST00000227251.3:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.126T>G
  hgvsp: ENST00000531198.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.126T>G
  hgvsp: ENST00000533971.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.126T>G
  hgvsp: ENST00000533879.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.126T>G
  hgvsp: ENST00000533475.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.126T>G
  hgvsp: ENST00000526180.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.126T>G
  hgvsp: ENST00000528628.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.126T>G
  hgvsp: ENST00000527950.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.126T>G
  hgvsp: ENST00000529647.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.126T>G
  hgvsp: ENST00000527899.1:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr42Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

11-111782325-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782325
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782325
    reference: chr 11
allele count: 1
allele frequency: 1.000980961342115e-5
allele num: 99902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.124A>G
  hgvsp: ENSP00000437149.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.124A>G
  hgvsp: ENSP00000435931.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.124A>G
  hgvsp: ENSP00000432182.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.124A>G
  hgvsp: ENSP00000434247.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.124A>G
  hgvsp: ENSP00000434269.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.124A>G
  hgvsp: ENSP00000436051.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.124A>G
  hgvsp: ENSP00000227251.3:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.124A>G
  hgvsp: ENSP00000431754.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.124A>G
  hgvsp: ENSP00000433560.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.124A>G
  hgvsp: ENSP00000436089.1:p.Thr42Ala
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25974
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr42Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

11-111782329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782329
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782329
    reference: chr 11
allele count: 3
allele frequency: 3.026329062846767e-5
allele num: 99130
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.120G>A
  hgvsp: ENST00000533475.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.120G>A
  hgvsp: ENST00000527950.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.120G>A
  hgvsp: ENST00000529647.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.120G>A
  hgvsp: ENST00000528628.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.120G>A
  hgvsp: ENST00000527899.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.120G>A
  hgvsp: ENST00000533971.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.120G>A
  hgvsp: ENST00000227251.3:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.120G>A
  hgvsp: ENST00000531198.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.120G>A
  hgvsp: ENST00000526180.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.120G>A
  hgvsp: ENST00000533879.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr40Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

11-111782330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782330
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782330
    reference: chr 11
allele count: 1
allele frequency: 1.012330181612035e-5
allele num: 98782
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.119C>T
  hgvsp: ENSP00000434247.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.119C>T
  hgvsp: ENSP00000436051.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.119C>T
  hgvsp: ENSP00000434269.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.119C>T
  hgvsp: ENSP00000437149.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.119C>T
  hgvsp: ENSP00000436089.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.119C>T
  hgvsp: ENSP00000432182.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.119C>T
  hgvsp: ENSP00000433560.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.119C>T
  hgvsp: ENSP00000227251.3:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.119C>T
  hgvsp: ENSP00000435931.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.119C>T
  hgvsp: ENSP00000431754.1:p.Thr40Met
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr40Met
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-111782332-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782332
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782332
    reference: chr 11
allele count: 1
allele frequency: 1.015104758811109e-5
allele num: 98512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.117G>A
  hgvsp: ENST00000527899.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.117G>A
  hgvsp: ENST00000533971.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.117G>A
  hgvsp: ENST00000526180.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.117G>A
  hgvsp: ENST00000533475.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.117G>A
  hgvsp: ENST00000527950.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.117G>A
  hgvsp: ENST00000531198.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.117G>A
  hgvsp: ENST00000227251.3:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.117G>A
  hgvsp: ENST00000529647.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.117G>A
  hgvsp: ENST00000528628.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.117G>A
  hgvsp: ENST00000533879.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro39Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

11-111782333-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782333
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782333
    reference: chr 11
allele count: 33
allele frequency: 3.359599291429967e-4
allele num: 98226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.116C>T
  hgvsp: ENSP00000434247.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.116C>T
  hgvsp: ENSP00000431754.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.116C>T
  hgvsp: ENSP00000433560.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.116C>T
  hgvsp: ENSP00000437149.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.116C>T
  hgvsp: ENSP00000227251.3:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.116C>T
  hgvsp: ENSP00000434269.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.116C>T
  hgvsp: ENSP00000432182.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.116C>T
  hgvsp: ENSP00000436051.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.116C>T
  hgvsp: ENSP00000435931.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.116C>T
  hgvsp: ENSP00000436089.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24322
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro39Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

11-111782334-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782334
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782334
    reference: chr 11
allele count: 3
allele frequency: 3.058602830227153e-5
allele num: 98084
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.115C>G
  hgvsp: ENSP00000433560.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.115C>G
  hgvsp: ENSP00000436089.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.115C>G
  hgvsp: ENSP00000227251.3:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.115C>G
  hgvsp: ENSP00000432182.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.115C>G
  hgvsp: ENSP00000436051.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.115C>G
  hgvsp: ENSP00000434269.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.115C>G
  hgvsp: ENSP00000434247.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.115C>G
  hgvsp: ENSP00000431754.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.115C>G
  hgvsp: ENSP00000435931.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.115C>G
  hgvsp: ENSP00000437149.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9068
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro39Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-111782353-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782353
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782353
    reference: chr 11
allele count: 1
allele frequency: 1.090155892292598e-5
allele num: 91730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.96G>T
  hgvsp: ENST00000531198.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.96G>T
  hgvsp: ENST00000533879.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.96G>T
  hgvsp: ENST00000527899.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.96G>T
  hgvsp: ENST00000227251.3:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.96G>T
  hgvsp: ENST00000526180.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.96G>T
  hgvsp: ENST00000528628.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.96G>T
  hgvsp: ENST00000529647.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.96G>T
  hgvsp: ENST00000527950.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.96G>T
  hgvsp: ENST00000533971.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.96G>T
  hgvsp: ENST00000533475.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu32Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

11-111782353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782353
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782353
    reference: chr 11
allele count: 1
allele frequency: 1.090155892292598e-5
allele num: 91730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.96G>A
  hgvsp: ENST00000531198.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.96G>A
  hgvsp: ENST00000527899.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.96G>A
  hgvsp: ENST00000227251.3:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.96G>A
  hgvsp: ENST00000533475.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.96G>A
  hgvsp: ENST00000528628.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.96G>A
  hgvsp: ENST00000527950.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.96G>A
  hgvsp: ENST00000526180.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.96G>A
  hgvsp: ENST00000529647.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.96G>A
  hgvsp: ENST00000533971.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.96G>A
  hgvsp: ENST00000533879.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18658
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu32Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

11-111782357-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782357
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782357
    reference: chr 11
allele count: 1
allele frequency: 1.105192192922349e-5
allele num: 90482
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.92A>C
  hgvsp: ENSP00000433560.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.92A>C
  hgvsp: ENSP00000431754.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.92A>C
  hgvsp: ENSP00000432182.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.92A>C
  hgvsp: ENSP00000437149.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.92A>C
  hgvsp: ENSP00000434247.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.92A>C
  hgvsp: ENSP00000227251.3:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.92A>C
  hgvsp: ENSP00000436051.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.92A>C
  hgvsp: ENSP00000436089.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.92A>C
  hgvsp: ENSP00000435931.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.92A>C
  hgvsp: ENSP00000434269.1:p.His31Pro
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His31Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

11-111782364-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782364
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782364
    reference: chr 11
allele count: 1
allele frequency: 1.13737176133391e-5
allele num: 87922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.85G>C
  hgvsp: ENSP00000437149.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.85G>C
  hgvsp: ENSP00000431754.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.85G>C
  hgvsp: ENSP00000433560.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.85G>C
  hgvsp: ENSP00000435931.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.85G>C
  hgvsp: ENSP00000436051.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.85G>C
  hgvsp: ENSP00000432182.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.85G>C
  hgvsp: ENSP00000436089.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.85G>C
  hgvsp: ENSP00000434247.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.85G>C
  hgvsp: ENSP00000434269.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.85G>C
  hgvsp: ENSP00000227251.3:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly29Arg
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

11-111782364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782364
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782364
    reference: chr 11
allele count: 4
allele frequency: 4.549487045335638e-5
allele num: 87922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.85G>A
  hgvsp: ENSP00000431754.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.85G>A
  hgvsp: ENSP00000227251.3:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.85G>A
  hgvsp: ENSP00000436051.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.85G>A
  hgvsp: ENSP00000436089.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.85G>A
  hgvsp: ENSP00000434269.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.85G>A
  hgvsp: ENSP00000432182.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.85G>A
  hgvsp: ENSP00000434247.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.85G>A
  hgvsp: ENSP00000437149.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.85G>A
  hgvsp: ENSP00000433560.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.85G>A
  hgvsp: ENSP00000435931.1:p.Gly29Arg
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17265
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly29Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

11-111782374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782374
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782374
    reference: chr 11
allele count: 2
allele frequency: 2.392001148160551e-5
allele num: 83612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.75C>G
  hgvsp: ENSP00000437149.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.75C>G
  hgvsp: ENSP00000433560.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.75C>G
  hgvsp: ENSP00000432182.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.75C>G
  hgvsp: ENSP00000434247.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.75C>G
  hgvsp: ENSP00000431754.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.75C>G
  hgvsp: ENSP00000434269.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.75C>G
  hgvsp: ENSP00000436089.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.75C>G
  hgvsp: ENSP00000436051.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.75C>G
  hgvsp: ENSP00000227251.3:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.75C>G
  hgvsp: ENSP00000435931.1:p.Asp25Glu
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp25Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-111782384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782384
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782384
    reference: chr 11
allele count: 1
allele frequency: 1.300863773545634e-5
allele num: 76872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.65G>A
  hgvsp: ENSP00000437149.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.65G>A
  hgvsp: ENSP00000433560.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.65G>A
  hgvsp: ENSP00000434269.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.65G>A
  hgvsp: ENSP00000227251.3:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.65G>A
  hgvsp: ENSP00000436051.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.65G>A
  hgvsp: ENSP00000434247.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.65G>A
  hgvsp: ENSP00000435931.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.65G>A
  hgvsp: ENSP00000432182.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.65G>A
  hgvsp: ENSP00000436089.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.65G>A
  hgvsp: ENSP00000431754.1:p.Arg22His
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg22His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-111782385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782385
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782385
    reference: chr 11
allele count: 2
allele frequency: 2.613832401066444e-5
allele num: 76516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.64C>T
  hgvsp: ENSP00000436089.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.64C>T
  hgvsp: ENSP00000434247.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.64C>T
  hgvsp: ENSP00000227251.3:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.64C>T
  hgvsp: ENSP00000437149.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.64C>T
  hgvsp: ENSP00000434269.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.64C>T
  hgvsp: ENSP00000432182.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.64C>T
  hgvsp: ENSP00000431754.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.64C>T
  hgvsp: ENSP00000436051.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.64C>T
  hgvsp: ENSP00000433560.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.64C>T
  hgvsp: ENSP00000435931.1:p.Arg22Cys
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13851
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg22Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

11-111782389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782389
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782389
    reference: chr 11
allele count: 607
allele frequency: 8.093117516866217e-3
allele num: 75002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.60C>T
  hgvsp: ENST00000227251.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.60C>T
  hgvsp: ENST00000528628.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.60C>T
  hgvsp: ENST00000527899.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.60C>T
  hgvsp: ENST00000533879.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.60C>T
  hgvsp: ENST00000531198.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.60C>T
  hgvsp: ENST00000527950.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.60C>T
  hgvsp: ENST00000526180.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.60C>T
  hgvsp: ENST00000533971.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.60C>T
  hgvsp: ENST00000533475.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.60C>T
  hgvsp: ENST00000529647.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21032
  bin: 7.5e0
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9816
  bin: 2.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13963
  bin: 1.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 267
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 1.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 2.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 5.25e1
  variant carriers: 2
hgvs: p.Pro20Pro
num of homozygotes: 14
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-111782389-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782389
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782389
    reference: chr 11
allele count: 2
allele frequency: 2.666595557451801e-5
allele num: 75002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.60C>G
  hgvsp: ENST00000533971.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.60C>G
  hgvsp: ENST00000533475.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.60C>G
  hgvsp: ENST00000531198.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.60C>G
  hgvsp: ENST00000533879.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.60C>G
  hgvsp: ENST00000527950.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.60C>G
  hgvsp: ENST00000529647.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.60C>G
  hgvsp: ENST00000527899.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.60C>G
  hgvsp: ENST00000528628.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.60C>G
  hgvsp: ENST00000526180.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.60C>G
  hgvsp: ENST00000227251.3:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9816
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro20Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

11-111782393-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782393
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782393
    reference: chr 11
allele count: 1
allele frequency: 1.379462561386084e-5
allele num: 72492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.56C>A
  hgvsp: ENSP00000436089.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.56C>A
  hgvsp: ENSP00000434247.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.56C>A
  hgvsp: ENSP00000433560.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.56C>A
  hgvsp: ENSP00000227251.3:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.56C>A
  hgvsp: ENSP00000431754.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.56C>A
  hgvsp: ENSP00000437149.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.56C>A
  hgvsp: ENSP00000436051.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.56C>A
  hgvsp: ENSP00000434269.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.56C>A
  hgvsp: ENSP00000435931.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.56C>A
  hgvsp: ENSP00000432182.1:p.Ser19Tyr
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser19Tyr
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-111782397-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782397
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782397
    reference: chr 11
allele count: 2
allele frequency: 2.855021983669274e-5
allele num: 70052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.52C>T
  hgvsp: ENSP00000434269.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.52C>T
  hgvsp: ENSP00000436089.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.52C>T
  hgvsp: ENSP00000432182.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.52C>T
  hgvsp: ENSP00000227251.3:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.52C>T
  hgvsp: ENSP00000435931.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.52C>T
  hgvsp: ENSP00000434247.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.52C>T
  hgvsp: ENSP00000436051.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.52C>T
  hgvsp: ENSP00000437149.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.52C>T
  hgvsp: ENSP00000433560.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.52C>T
  hgvsp: ENSP00000431754.1:p.His18Tyr
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14372
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His18Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

11-111782404-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782404
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782404
    reference: chr 11
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.45T>C
  hgvsp: ENST00000531198.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.45T>C
  hgvsp: ENST00000533971.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.45T>C
  hgvsp: ENST00000527899.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.45T>C
  hgvsp: ENST00000227251.3:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.45T>C
  hgvsp: ENST00000526180.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.45T>C
  hgvsp: ENST00000527950.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.45T>C
  hgvsp: ENST00000528628.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.45T>C
  hgvsp: ENST00000533879.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.45T>C
  hgvsp: ENST00000529647.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.45T>C
  hgvsp: ENST00000533475.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe15Phe
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-111782415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782415
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782415
    reference: chr 11
allele count: 3
allele frequency: 5.253020486779898e-5
allele num: 57110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.34C>T
  hgvsp: ENSP00000436089.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.34C>T
  hgvsp: ENSP00000437149.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.34C>T
  hgvsp: ENSP00000227251.3:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.34C>T
  hgvsp: ENSP00000436051.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.34C>T
  hgvsp: ENSP00000433560.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.34C>T
  hgvsp: ENSP00000432182.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.34C>T
  hgvsp: ENSP00000431754.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.34C>T
  hgvsp: ENSP00000435931.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.34C>T
  hgvsp: ENSP00000434247.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.34C>T
  hgvsp: ENSP00000434269.1:p.Arg12Cys
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2425
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg12Cys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

11-111782416-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782416
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782416
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 57176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.33C>G
  hgvsp: ENST00000526180.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.33C>G
  hgvsp: ENST00000227251.3:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.33C>G
  hgvsp: ENST00000531198.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.33C>G
  hgvsp: ENST00000527950.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.33C>G
  hgvsp: ENST00000533475.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.33C>G
  hgvsp: ENST00000533971.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.33C>G
  hgvsp: ENST00000533879.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.33C>G
  hgvsp: ENST00000529647.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.33C>G
  hgvsp: ENST00000528628.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.33C>G
  hgvsp: ENST00000527899.1:c.33C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26015
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg11Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

11-111782417-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782417
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782417
    reference: chr 11
allele count: 2
allele frequency: 3.554797198819808e-5
allele num: 56262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.32G>A
  hgvsp: ENSP00000434269.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.32G>A
  hgvsp: ENSP00000436051.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.32G>A
  hgvsp: ENSP00000437149.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.32G>A
  hgvsp: ENSP00000436089.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.32G>A
  hgvsp: ENSP00000227251.3:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.32G>A
  hgvsp: ENSP00000434247.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.32G>A
  hgvsp: ENSP00000433560.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.32G>A
  hgvsp: ENSP00000431754.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.32G>A
  hgvsp: ENSP00000432182.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.32G>A
  hgvsp: ENSP00000435931.1:p.Arg11His
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14114
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg11His
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-111782418-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782418
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782418
    reference: chr 11
allele count: 1
allele frequency: 1.838370468416796e-5
allele num: 54396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.31C>T
  hgvsp: ENSP00000433560.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.31C>T
  hgvsp: ENSP00000436051.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.31C>T
  hgvsp: ENSP00000436089.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.31C>T
  hgvsp: ENSP00000437149.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.31C>T
  hgvsp: ENSP00000227251.3:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.31C>T
  hgvsp: ENSP00000431754.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.31C>T
  hgvsp: ENSP00000434247.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.31C>T
  hgvsp: ENSP00000434269.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.31C>T
  hgvsp: ENSP00000432182.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.31C>T
  hgvsp: ENSP00000435931.1:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6476
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg11Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

11-111782422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782422
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782422
    reference: chr 11
allele count: 1
allele frequency: 1.893867656528162e-5
allele num: 52802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.27G>A
  hgvsp: ENSP00000436051.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.27G>A
  hgvsp: ENSP00000434269.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.27G>A
  hgvsp: ENSP00000436089.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.27G>A
  hgvsp: ENSP00000437149.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.27G>A
  hgvsp: ENSP00000435931.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.27G>A
  hgvsp: ENSP00000227251.3:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.27G>A
  hgvsp: ENSP00000432182.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.27G>A
  hgvsp: ENSP00000434247.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.27G>A
  hgvsp: ENSP00000431754.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.27G>A
  hgvsp: ENSP00000433560.1:p.Trp9Ter
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp9Ter
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

11-111782427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782427
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782427
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 49094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.22C>T
  hgvsp: ENSP00000227251.3:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.22C>T
  hgvsp: ENSP00000434269.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.22C>T
  hgvsp: ENSP00000436089.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.22C>T
  hgvsp: ENSP00000432182.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.22C>T
  hgvsp: ENSP00000434247.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.22C>T
  hgvsp: ENSP00000431754.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.22C>T
  hgvsp: ENSP00000433560.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.22C>T
  hgvsp: ENSP00000436051.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.22C>T
  hgvsp: ENSP00000437149.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.22C>T
  hgvsp: ENSP00000435931.1:p.Pro8Ser
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26694
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5124
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro8Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-111782431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782431
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782431
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 46594
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.18C>T
  hgvsp: ENST00000533475.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.18C>T
  hgvsp: ENST00000533879.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.18C>T
  hgvsp: ENST00000531198.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.18C>T
  hgvsp: ENST00000527899.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.18C>T
  hgvsp: ENST00000526180.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.18C>T
  hgvsp: ENST00000527950.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.18C>T
  hgvsp: ENST00000227251.3:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.18C>T
  hgvsp: ENST00000528628.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.18C>T
  hgvsp: ENST00000533971.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.18C>T
  hgvsp: ENST00000529647.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26942
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His6His
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-111782442-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782442
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782442
    reference: chr 11
allele count: 1
allele frequency: 2.426477724934485e-5
allele num: 41212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.7A>G
  hgvsp: ENSP00000434247.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.7A>G
  hgvsp: ENSP00000435931.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.7A>G
  hgvsp: ENSP00000227251.3:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.7A>G
  hgvsp: ENSP00000437149.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.7A>G
  hgvsp: ENSP00000432182.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.7A>G
  hgvsp: ENSP00000436051.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.7A>G
  hgvsp: ENSP00000434269.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.7A>G
  hgvsp: ENSP00000436089.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.7A>G
  hgvsp: ENSP00000433560.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.7A>G
  hgvsp: ENSP00000431754.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile3Val
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

11-111782443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782443
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782443
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 40802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.6C>T
  hgvsp: ENST00000527899.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.6C>T
  hgvsp: ENST00000529647.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.6C>T
  hgvsp: ENST00000526180.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.6C>T
  hgvsp: ENST00000533879.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.6C>T
  hgvsp: ENST00000527950.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.6C>T
  hgvsp: ENST00000533475.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.6C>T
  hgvsp: ENST00000531198.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.6C>T
  hgvsp: ENST00000227251.3:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.6C>T
  hgvsp: ENST00000528628.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.6C>T
  hgvsp: ENST00000533971.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26076
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13523
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp2Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-111782445-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782445
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782445
    reference: chr 11
allele count: 1
allele frequency: 2.488304966656714e-5
allele num: 40188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.4G>A
  hgvsp: ENSP00000227251.3:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.4G>A
  hgvsp: ENSP00000433560.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.4G>A
  hgvsp: ENSP00000434269.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.4G>A
  hgvsp: ENSP00000435931.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.4G>A
  hgvsp: ENSP00000431754.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.4G>A
  hgvsp: ENSP00000437149.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.4G>A
  hgvsp: ENSP00000436051.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.4G>A
  hgvsp: ENSP00000434247.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.4G>A
  hgvsp: ENSP00000432182.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.4G>A
  hgvsp: ENSP00000436089.1:p.Asp2Asn
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp2Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

11-111782446-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782446
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782446
    reference: chr 11
allele count: 3
allele frequency: 7.561627262186823e-5
allele num: 39674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.3G>A
  hgvsp: ENSP00000431754.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.3G>A
  hgvsp: ENSP00000434247.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.3G>A
  hgvsp: ENSP00000433560.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.3G>A
  hgvsp: ENSP00000436051.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.3G>A
  hgvsp: ENSP00000435931.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.3G>A
  hgvsp: ENSP00000227251.3:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.3G>A
  hgvsp: ENSP00000434269.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.3G>A
  hgvsp: ENSP00000436089.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.3G>A
  hgvsp: ENSP00000437149.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.3G>A
  hgvsp: ENSP00000432182.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25781
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13895
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9771
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Met1?
num of homozygotes: 1
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

11-111782447-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782447
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782447
    reference: chr 11
allele count: 1
allele frequency: 2.53434031121699e-5
allele num: 39458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.2T>C
  hgvsp: ENSP00000431754.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.2T>C
  hgvsp: ENSP00000432182.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.2T>C
  hgvsp: ENSP00000434269.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.2T>C
  hgvsp: ENSP00000227251.3:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.2T>C
  hgvsp: ENSP00000436051.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.2T>C
  hgvsp: ENSP00000435931.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.2T>C
  hgvsp: ENSP00000436089.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.2T>C
  hgvsp: ENSP00000433560.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.2T>C
  hgvsp: ENSP00000434247.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.2T>C
  hgvsp: ENSP00000437149.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25570
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met1?
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: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

11-111782449-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782449
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782449
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 37600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24596
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16437
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-111782450-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782450
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782450
    reference: chr 11
allele count: 1
allele frequency: 2.660565104028095e-5
allele num: 37586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.-2C>G
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25510
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-111782454-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782454
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782454
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 35930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24168
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4200
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-111782457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782457
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782457
    reference: chr 11
allele count: 2
allele frequency: 5.743495491356039e-5
allele num: 34822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23651
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4174
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-111782468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782468
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782468
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 29296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20427
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16234
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3081
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-111782469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782469
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782469
    reference: chr 11
allele count: 18
allele frequency: 6.149221098660836e-4
allele num: 29272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  hgvsc: ENST00000531198.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  hgvsc: ENST00000527899.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  hgvsc: ENST00000526180.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  hgvsc: ENST00000533475.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  hgvsc: ENST00000527950.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  hgvsc: ENST00000533879.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  hgvsc: ENST00000533971.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  hgvsc: ENST00000528628.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  hgvsc: ENST00000529647.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  hgvsc: ENST00000227251.3:c.-21C>T
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23569
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20468
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3847
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24497
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

11-111782469-GGGTCAGCTGGCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 111782469
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 111782457
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 29272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000227251
  ensembl transcript: ENST00000227251
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436089
  ensembl transcript: ENST00000527899
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000437149
  ensembl transcript: ENST00000527950
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434247
  ensembl transcript: ENST00000531198
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000432182
  ensembl transcript: ENST00000528628
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000431754
  ensembl transcript: ENST00000529647
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000435931
  ensembl transcript: ENST00000533879
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000433560
  ensembl transcript: ENST00000533475
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000436051
  ensembl transcript: ENST00000526180
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109846
  ensembl protein: ENSP00000434269
  ensembl transcript: ENST00000533971
  gene symbol: CRYAB
  variant of: http://identifiers.org/hgnc/2389
canonical: true
consequence: 5' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20468
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16627
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24497
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: GGGTCAGCTGGCT
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

GenotypeDepth
all individuals: 2732
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8871
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 720
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1755
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 621
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6286
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2598
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19958
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22539
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.642e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.354092e6

MQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.19e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeDepth
all individuals: 1303
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2600
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2219
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 718
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5266
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2594
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22515
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19955
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2084
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
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: 8648
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.658e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 3.784e0

DP
type: SiteQuality
SIO_000300: 2.353057e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.064e0

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeDepth
all individuals: 22258
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1757
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 3192
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1302
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2605
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22476
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19964
bin: 9.75e1
variant carriers: 16

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: 66718
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: 8646
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 17
allele frequency: 1.029554263565892e-3
allele num: 16512
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.97e-1

DP
type: SiteQuality
SIO_000300: 2.353535e6

FS
type: SiteQuality
SIO_000300: 2.133e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

QD
type: SiteQuality
SIO_000300: 1.515e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 6.57e-1

GenotypeDepth
all individuals: 2629
bin: 9.75e1
variant carriers: 39

GenotypeDepth
all individuals: 8827
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3508
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 2732
bin: 5.25e1
variant carriers: 5

GenotypeDepth
all individuals: 720
bin: 7.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20022
bin: 9.75e1
variant carriers: 91

GenotypeQuality
all individuals: 2585
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22303
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2079
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 90
allele frequency: 1.349042180052163e-3
allele num: 66714
num of homozygotes: 1

African
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allele frequency: 1.922337562475971e-4
allele num: 10404
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Other
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num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66706
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Latino
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European (Finnish)
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Other
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VQSLOD
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DP
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QD
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

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

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

European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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Other
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QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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African
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Latino
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Other
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QD
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VQSLOD
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MQ
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FS
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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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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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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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QD
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BaseQRankSum
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DP
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1509
bin: 6.75e1
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GenotypeQuality
all individuals: 2522
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3522
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

DP
type: SiteQuality
SIO_000300: 7.49142e5

QD
type: SiteQuality
SIO_000300: 1.416e1

GenotypeQuality
all individuals: 6533
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.563537880407669e-5
allele num: 28062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2156
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

QD
type: SiteQuality
SIO_000300: 1.059e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

DP
type: SiteQuality
SIO_000300: 8.13569e5

FS
type: SiteQuality
SIO_000300: 1.169e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 1951
bin: 9.75e1
variant carriers: 2

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1978
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.563537880407669e-5
allele num: 28062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.817520901490367e-4
allele num: 5502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

DP
type: SiteQuality
SIO_000300: 8.13569e5

QD
type: SiteQuality
SIO_000300: 1.059e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

FS
type: SiteQuality
SIO_000300: 1.169e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1730
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variant carriers: 0

GenotypeQuality
all individuals: 4348
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.76056338028169e-4
allele num: 5680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.393741939862893e-5
allele num: 29466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-2

QD
type: SiteQuality
SIO_000300: 1.602e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

FS
type: SiteQuality
SIO_000300: 7.793e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

DP
type: SiteQuality
SIO_000300: 8.50428e5

GenotypeQuality
all individuals: 4147
bin: 3.25e1
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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variant carriers: 3

GenotypeQuality
all individuals: 391
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GenotypeQuality
all individuals: 668
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.946661475569399e-4
allele num: 10274
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.880429477794046e-4
allele num: 4098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2154
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 8.103727714748784e-4
allele num: 2468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.555478741790529e-3
allele num: 5786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.641429235571495e-5
allele num: 30114
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

FS
type: SiteQuality
SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 8.64971e5

QD
type: SiteQuality
SIO_000300: 1.214e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.101159833777833e-5
allele num: 32246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4368
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2818
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.951e0

FS
type: SiteQuality
SIO_000300: 3.757e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

DP
type: SiteQuality
SIO_000300: 9.03666e5

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 5.753e1

MQRankSum
type: SiteQuality
SIO_000300: -1.775e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.13195977434388e-5
allele num: 32616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

DP
type: SiteQuality
SIO_000300: 9.11166e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 402
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.13195977434388e-5
allele num: 32616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 9.11166e5

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.31e0

GenotypeQuality
all individuals: 711
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 509
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GenotypeQuality
all individuals: 233
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GenotypeQuality
all individuals: 2061
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GenotypeQuality
all individuals: 464
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GenotypeQuality
all individuals: 736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13817
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.931519699812383e-5
allele num: 34112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4586
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.596e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 9.36305e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.379e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 7.5e0
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GenotypeQuality
all individuals: 316
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18732
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11854
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.616553507921112e-4
allele num: 6186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.37e-1

MQ
type: SiteQuality
SIO_000300: 5.797e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.024e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e0

DP
type: SiteQuality
SIO_000300: 1.145884e6

GenotypeQuality
all individuals: 274
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.5e0
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GenotypeQuality
all individuals: 1963
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 4.25e1
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GenotypeQuality
all individuals: 234
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variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.98358761900968e-5
allele num: 50206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.566e0

MQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.183165e6

FS
type: SiteQuality
SIO_000300: 4.458e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 3.45e-1

GenotypeQuality
all individuals: 894
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14642
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 887
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variant carriers: 0

GenotypeQuality
all individuals: 693
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variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3099
bin: 6.75e1
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GenotypeQuality
all individuals: 489
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31169
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.594706798131811e-4
allele num: 7708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.76548555936288e-5
allele num: 53114
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

FS
type: SiteQuality
SIO_000300: 3.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

DP
type: SiteQuality
SIO_000300: 1.232495e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -7.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.135e0

GenotypeQuality
all individuals: 736
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
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variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3154
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14293
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
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variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31070
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.865741259002202e-5
allele num: 53598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8070
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6942
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.256e1

DP
type: SiteQuality
SIO_000300: 1.238724e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 3.111e0

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.617e0

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 262
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 1964
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variant carriers: 1

GenotypeQuality
all individuals: 1321
bin: 2.75e1
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GenotypeQuality
all individuals: 539
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GenotypeQuality
all individuals: 245
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GenotypeQuality
all individuals: 32693
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GenotypeQuality
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GenotypeQuality
all individuals: 978
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GenotypeQuality
all individuals: 288
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GenotypeQuality
all individuals: 1247
bin: 3.25e1
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GenotypeQuality
all individuals: 493
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GenotypeQuality
all individuals: 13208
bin: 2.25e1
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GenotypeQuality
all individuals: 683
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
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variant carriers: 0

GenotypeQuality
all individuals: 956
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variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.226993865030675e-4
allele num: 8150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7112
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.061e0

DP
type: SiteQuality
SIO_000300: 1.265808e6

MQRankSum
type: SiteQuality
SIO_000300: -3.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.56e-1

QD
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

GenotypeQuality
all individuals: 730
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 377
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 178
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 32881
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 12303
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 244
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variant carriers: 14

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1115
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 482
bin: 8.25e1
variant carriers: 14

GenotypeQuality
all individuals: 781
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3495
bin: 9.75e1
variant carriers: 1782

GenotypeQuality
all individuals: 959
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variant carriers: 10

GenotypeQuality
all individuals: 3212
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 290
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variant carriers: 14

GenotypeQuality
all individuals: 626
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 963
bin: 7.25e1
variant carriers: 8

Latino
type: Population
allele count: 45
allele frequency: 5.3712103127238e-3
allele num: 8378
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 3.962536023054755e-3
allele num: 8328
num of homozygotes: 1

East Asian
type: Population
allele count: 2
allele frequency: 2.773925104022191e-4
allele num: 7210
num of homozygotes: 0

South Asian
type: Population
allele count: 414
allele frequency: 3.150205448181403e-2
allele num: 13142
num of homozygotes: 10

Other
type: Population
allele count: 12
allele frequency: 1.759530791788856e-2
allele num: 682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 92
allele frequency: 2.085222121486854e-2
allele num: 4412
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 1300
allele frequency: 2.323253985274144e-2
allele num: 55956
num of homozygotes: 18

QD
type: SiteQuality
SIO_000300: 1.201e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.967e0

DP
type: SiteQuality
SIO_000300: 1.310632e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

FS
type: SiteQuality
SIO_000300: 5.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

GenotypeQuality
all individuals: 486
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
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GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 1261
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 155
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GenotypeQuality
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GenotypeQuality
all individuals: 469
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GenotypeQuality
all individuals: 1160
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GenotypeQuality
all individuals: 904
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 9.25e1
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GenotypeQuality
all individuals: 1008
bin: 7.75e1
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GenotypeQuality
all individuals: 33627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 7.66951368310964e-4
allele num: 57370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4560
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.176747469992939e-4
allele num: 8498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13336
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

DP
type: SiteQuality
SIO_000300: 1.297598e6

FS
type: SiteQuality
SIO_000300: 1.105e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.71e-1

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 969
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.739614501426484e-5
allele num: 57484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4594
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.300243e6

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.204e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

GenotypeQuality
all individuals: 1286
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 987
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7366
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.434944237918216e-5
allele num: 13450
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.300641e6

FS
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.117e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.244e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.737740242588538e-5
allele num: 57546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

FS
type: SiteQuality
SIO_000300: 9.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 5.77e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.468e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.296386e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13335
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 460
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variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.256518082422203e-5
allele num: 57072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

DP
type: SiteQuality
SIO_000300: 1.283235e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.872e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.009e1

GenotypeQuality
all individuals: 1515
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31168
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.758396342535608e-5
allele num: 56870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.277741e6

FS
type: SiteQuality
SIO_000300: 2.943e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.677e1

VQSLOD
type: SiteQuality
SIO_000300: 3.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

African
type: Population
allele count: 2
allele frequency: 2.378686964795433e-4
allele num: 8408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.501875468867217e-5
allele num: 13330
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

QD
type: SiteQuality
SIO_000300: 1.409e1

FS
type: SiteQuality
SIO_000300: 6.878e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 13290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.777272242562116e-5
allele num: 56266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4490
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.263342e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.429999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.02e0

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -7.65e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 619
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GenotypeQuality
all individuals: 148
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variant carriers: 0

Latino
type: Population
allele count: 0
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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South Asian
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Other
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ReadPosRankSum
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ClippingRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Latino
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Other
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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SIO_000300: 1.6e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Other
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European (Non-Finnish)
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South Asian
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Latino
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QD
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -3.7e-1

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

European (Finnish)
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European (Non-Finnish)
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Other
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African
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East Asian
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South Asian
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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DP
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 51978
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Other
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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MQRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Other
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East Asian
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African
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Latino
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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Latino
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ReadPosRankSum
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FS
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VQSLOD
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DP
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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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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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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Other
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South Asian
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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QD
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 2
allele frequency: 5.47945205479452e-4
allele num: 3650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47020
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

FS
type: SiteQuality
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QD
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InbreedingCoeff
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VQSLOD
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SIO_000300: 1.3e0

MQRankSum
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SIO_000300: 2.72e-1

ReadPosRankSum
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SIO_000300: -6.34e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

ClippingRankSum
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SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 1.078373e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12100
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42846
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.45900204260286e-4
allele num: 6854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3200
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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DP
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VQSLOD
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SIO_000300: -4.044e-1

ReadPosRankSum
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SIO_000300: 2.28e0

ClippingRankSum
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QD
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SIO_000300: 1.048e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 562
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.34587595007976e-5
allele num: 42628
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5652
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South Asian
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allele count: 1
allele frequency: 8.280887711162637e-5
allele num: 12076
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VQSLOD
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SIO_000300: -1.395e0

BaseQRankSum
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MQ
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FS
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QD
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SIO_000300: 7.77e0

ClippingRankSum
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SIO_000300: -6.34e-1

DP
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SIO_000300: 1.00238e6

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 587

GenotypeQuality
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variant carriers: 8

Other
type: Population
allele count: 5
allele frequency: 9.09090909090909e-3
allele num: 550
num of homozygotes: 0

South Asian
type: Population
allele count: 584
allele frequency: 4.843257588323105e-2
allele num: 12058
num of homozygotes: 14

European (Finnish)
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allele count: 1
allele frequency: 3.248862897985705e-4
allele num: 3078
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.922337562475971e-4
allele num: 41616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

Latino
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allele count: 9
allele frequency: 1.639941690962099e-3
allele num: 5488
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

VQSLOD
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SIO_000300: 6.07e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.99e1

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.01682e6

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41616
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.658649859014762e-4
allele num: 12058
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6710
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

QD
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FS
type: SiteQuality
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.11e-2

ClippingRankSum
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DP
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MQRankSum
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MQ
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SIO_000300: 5.99e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
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allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5254
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 8.59697386519945e-5
allele num: 11632
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40220
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InbreedingCoeff
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SIO_000300: -6.9e-3

BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 5.148800329523221e-5
allele num: 38844
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African
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allele count: 0
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South Asian
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VQSLOD
type: SiteQuality
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.723163226403791e-5
allele num: 36722
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.096e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

FS
type: SiteQuality
SIO_000300: 2.017e0

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

DP
type: SiteQuality
SIO_000300: 9.03797e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

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: 2

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5430
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.904036557501904e-4
allele num: 10504
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.214813862277374e-5
allele num: 31106
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.41e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3588
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4140
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31118
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 6.854e0

DP
type: SiteQuality
SIO_000300: 8.26451e5

QD
type: SiteQuality
SIO_000300: 9.56e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.315e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 750
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.546216286986122e-5
allele num: 30552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

QD
type: SiteQuality
SIO_000300: 9.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.152e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

DP
type: SiteQuality
SIO_000300: 8.25548e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3274
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1786
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3918
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 29456
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.714396735962697e-5
allele num: 10294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.11661e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.098e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-1

QD
type: SiteQuality
SIO_000300: 1.512e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3106
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.516669011112674e-5
allele num: 28436
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
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DP
type: SiteQuality
SIO_000300: 7.9954e5

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.871e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -8.149999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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Latino
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allele frequency: 0.0e0
allele num: 2684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3526
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
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MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3352
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2396
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 24786
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
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MQRankSum
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QD
type: SiteQuality
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FS
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

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

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

European (Non-Finnish)
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allele frequency: 4.635638791025404e-5
allele num: 21572
num of homozygotes: 0

East Asian
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South Asian
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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SIO_000300: -2.09e-1

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

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

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2880
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: 0
allele frequency: 0.0e0
allele num: 21312
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 20968
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele num: 2802
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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MQ
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 4138
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1004
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.093294460641399e-3
allele num: 2744
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
type: Population
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 1.098901098901099e-4
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European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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Other
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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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MQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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African
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South Asian
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East Asian
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FS
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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Other
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MQ
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FS
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18970
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2320
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.886435331230284e-4
allele num: 1268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.672793283412752e-5
allele num: 17628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.895e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.62e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.596e5

FS
type: SiteQuality
SIO_000300: 1.2914e1

QD
type: SiteQuality
SIO_000300: 1.563e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

GenotypeQuality
all individuals: 24420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2949
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.678e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.06867e5

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.67e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 854
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 618
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 666
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3055
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2592
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1514
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 6.406605922551253e-4
allele num: 14048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 1.065845570819517e-3
allele num: 8444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.77e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.463e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

FS
type: SiteQuality
SIO_000300: 8.83e-1

DP
type: SiteQuality
SIO_000300: 6.05971e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeQuality
all individuals: 854
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3847
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1683
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2592
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.463e1

FS
type: SiteQuality
SIO_000300: 8.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.77e-2