16-30081074-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081074
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081074
    reference: chr 16
allele count: 1
allele frequency: 8.753348155669544e-6
allele num: 114242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-77A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-77A>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-30081080-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081080
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081080
    reference: chr 16
allele count: 2
allele frequency: 1.750914853010698e-5
allele num: 114226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-71A>C
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11423
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-30081080-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081080
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081080
    reference: chr 16
allele count: 3
allele frequency: 2.626372279516047e-5
allele num: 114226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-71A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-71A>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

16-30081083-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081083
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081082
    reference: chr 16
allele count: 2
allele frequency: 1.750301927082422e-5
allele num: 114266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-66delC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-66delC
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: TC
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

16-30081088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081088
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081088
    reference: chr 16
allele count: 91
allele frequency: 7.944822769338222e-4
allele num: 114540
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-63C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14872
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11201
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-30081093-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081093
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081093
    reference: chr 16
allele count: 1
allele frequency: 8.692779777117127e-6
allele num: 115038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-58C>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17028
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

16-30081096-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081096
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081096
    reference: chr 16
allele count: 1
allele frequency: 8.693837807761858e-6
allele num: 115024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-55G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-55G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-30081102-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081102
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081102
    reference: chr 16
allele count: 1
allele frequency: 8.641100530563572e-6
allele num: 115726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-49T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-49T>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-30081105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081105
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081105
    reference: chr 16
allele count: 2
allele frequency: 1.725834009284987e-5
allele num: 115886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-46C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-46C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-30081107-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081107
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081107
    reference: chr 16
allele count: 1
allele frequency: 8.621135575978068e-6
allele num: 115994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-44G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-44G>C
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-30081120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081120
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081120
    reference: chr 16
allele count: 3
allele frequency: 2.546905509805586e-5
allele num: 117790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-31C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23863
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-30081122-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081122
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081123
    reference: chr 16
allele count: 2
allele frequency: 1.693939085950469e-5
allele num: 118068
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-25dupC
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14884
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/16-30081124-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081124
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081124
    reference: chr 16
allele count: 1
allele frequency: 8.442238206193226e-6
allele num: 118452
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-27C>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

16-30081125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081125
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081125
    reference: chr 16
allele count: 1
allele frequency: 8.436113313874031e-6
allele num: 118538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-26C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-26C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15279
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-30081130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081130
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081130
    reference: chr 16
allele count: 4
allele frequency: 3.357732858773756e-5
allele num: 119128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-21C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-21C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15667
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-30081131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081131
    reference: chr 16
allele count: 31
allele frequency: 2.598621892132044e-4
allele num: 119294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-20G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-20G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15777
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

16-30081137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081137
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081137
    reference: chr 16
allele count: 2
allele frequency: 1.66908684258842e-5
allele num: 119826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-14C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-30081138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081138
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081138
    reference: chr 16
allele count: 1
allele frequency: 8.340561820244212e-6
allele num: 119896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-13C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-13C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-30081140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081140
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081140
    reference: chr 16
allele count: 4
allele frequency: 3.333166674999583e-5
allele num: 120006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-11C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-11C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25246
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16311
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

16-30081144-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081144
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081144
    reference: chr 16
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-7T>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-7T>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.962-7T>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/16-30081148-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081149
    reference: chr 16
allele count: 3
allele frequency: 2.49214972835568e-5
allele num: 120378
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97-2dupA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304-2dupA
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.962-2dupA
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

16-30081151-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081151
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081151
    reference: chr 16
allele count: 5
allele frequency: 4.150341988179826e-5
allele num: 120472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.962G>C
  hgvsp: ENSP00000457468.2:p.Gly321Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.800G>C
  hgvsp: ENSP00000455857.1:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.800G>C
  hgvsp: ENSP00000336927.5:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.812G>C
  hgvsp: ENSP00000378661.3:p.Gly271Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.800G>C
  hgvsp: ENSP00000400452.2:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.800G>C
  hgvsp: ENSP00000455724.1:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1994G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.800G>C
  hgvsp: ENSP00000455700.1:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.97G>C
  hgvsp: ENSP00000456098.1:p.Gly33Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.800G>C
  hgvsp: ENSP00000455800.2:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.800G>C
  hgvsp: ENSP00000455917.1:p.Gly267Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.962G>C
  hgvsp: ENSP00000378669.1:p.Gly321Ala
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.304G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.551G>C
  hgvsp: ENSP00000457514.1:p.Gly184Ala
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly321Ala
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

16-30081152-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081152
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081152
    reference: chr 16
allele count: 1
allele frequency: 8.298204268596276e-6
allele num: 120508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.801G>A
  hgvsp: ENST00000564546.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.305G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.813G>A
  hgvsp: ENST00000395240.3:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.801G>A
  hgvsp: ENST00000569798.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.963G>A
  hgvsp: ENST00000395248.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.801G>A
  hgvsp: ENST00000563060.2:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.963G>A
  hgvsp: ENST00000564595.2:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.801G>A
  hgvsp: ENST00000412304.2:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1995G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.552G>A
  hgvsp: ENST00000564688.1:c.552G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.801G>A
  hgvsp: ENST00000569545.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.98G>A
  hgvsp: ENST00000565355.1:c.98G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.801G>A
  hgvsp: ENST00000338110.5:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.801G>A
  hgvsp: ENST00000566897.1:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.963G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

16-30081152-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081152
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081152
    reference: chr 16
allele count: 6
allele frequency: 4.978922561157765e-5
allele num: 120508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.552G>C
  hgvsp: ENST00000564688.1:c.552G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.801G>C
  hgvsp: ENST00000569798.1:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.801G>C
  hgvsp: ENST00000569545.1:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.963G>C
  hgvsp: ENST00000395248.1:c.963G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.963G>C
  hgvsp: ENST00000564595.2:c.963G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.813G>C
  hgvsp: ENST00000395240.3:c.813G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.801G>C
  hgvsp: ENST00000412304.2:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1995G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.98G>C
  hgvsp: ENST00000565355.1:c.98G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.801G>C
  hgvsp: ENST00000566897.1:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.305G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.801G>C
  hgvsp: ENST00000564546.1:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.801G>C
  hgvsp: ENST00000563060.2:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.801G>C
  hgvsp: ENST00000338110.5:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16676
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.963G>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-30081155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081155
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081155
    reference: chr 16
allele count: 6
allele frequency: 4.975949577044286e-5
allele num: 120580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.804C>T
  hgvsp: ENST00000569545.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.804C>T
  hgvsp: ENST00000564546.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.804C>T
  hgvsp: ENST00000563060.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.804C>T
  hgvsp: ENST00000569798.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.555C>T
  hgvsp: ENST00000564688.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.804C>T
  hgvsp: ENST00000338110.5:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.966C>T
  hgvsp: ENST00000564595.2:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.1998C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.816C>T
  hgvsp: ENST00000395240.3:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.101C>T
  hgvsp: ENST00000565355.1:c.101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.966C>T
  hgvsp: ENST00000395248.1:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.804C>T
  hgvsp: ENST00000566897.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.804C>T
  hgvsp: ENST00000412304.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.308C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile322Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

16-30081162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081162
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081162
    reference: chr 16
allele count: 140
allele frequency: 1.159669991053974e-3
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.973C>T
  hgvsp: ENST00000564595.2:c.973C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.811C>T
  hgvsp: ENST00000412304.2:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.108C>T
  hgvsp: ENST00000565355.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.811C>T
  hgvsp: ENST00000338110.5:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.811C>T
  hgvsp: ENST00000569545.1:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.562C>T
  hgvsp: ENST00000564688.1:c.562C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.811C>T
  hgvsp: ENST00000564546.1:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.973C>T
  hgvsp: ENST00000395248.1:c.973C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2005C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.811C>T
  hgvsp: ENST00000566897.1:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.811C>T
  hgvsp: ENST00000563060.2:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.823C>T
  hgvsp: ENST00000395240.3:c.823C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.315C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.811C>T
  hgvsp: ENST00000569798.1:c.811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25664
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8279
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Leu325Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS

16-30081164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081164
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081164
    reference: chr 16
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.975G>A
  hgvsp: ENST00000395248.1:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.825G>A
  hgvsp: ENST00000395240.3:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2007G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.813G>A
  hgvsp: ENST00000412304.2:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.813G>A
  hgvsp: ENST00000569798.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.813G>A
  hgvsp: ENST00000338110.5:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.110G>A
  hgvsp: ENST00000565355.1:c.110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.317G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.564G>A
  hgvsp: ENST00000564688.1:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.813G>A
  hgvsp: ENST00000569545.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.813G>A
  hgvsp: ENST00000563060.2:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.975G>A
  hgvsp: ENST00000564595.2:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.813G>A
  hgvsp: ENST00000566897.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.813G>A
  hgvsp: ENST00000564546.1:c.813G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu325Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

16-30081177-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081177
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081177
    reference: chr 16
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.330A>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.826A>T
  hgvsp: ENSP00000455700.1:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.826A>T
  hgvsp: ENSP00000455917.1:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.826A>T
  hgvsp: ENSP00000336927.5:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.988A>T
  hgvsp: ENSP00000378669.1:p.Ser330Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.826A>T
  hgvsp: ENSP00000400452.2:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.826A>T
  hgvsp: ENSP00000455800.2:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2020A>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.988A>T
  hgvsp: ENSP00000457468.2:p.Ser330Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.838A>T
  hgvsp: ENSP00000378661.3:p.Ser280Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.577A>T
  hgvsp: ENSP00000457514.1:p.Ser193Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.826A>T
  hgvsp: ENSP00000455857.1:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.123A>T
  hgvsp: ENSP00000456098.1:p.Ser42Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.826A>T
  hgvsp: ENSP00000455724.1:p.Ser276Cys
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser330Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

16-30081184-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081184
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081184
    reference: chr 16
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2027A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.833A>G
  hgvsp: ENSP00000336927.5:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.833A>G
  hgvsp: ENSP00000400452.2:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.833A>G
  hgvsp: ENSP00000455800.2:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.833A>G
  hgvsp: ENSP00000455700.1:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.845A>G
  hgvsp: ENSP00000378661.3:p.Glu282Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.833A>G
  hgvsp: ENSP00000455857.1:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.995A>G
  hgvsp: ENSP00000378669.1:p.Glu332Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.130A>G
  hgvsp: ENSP00000456098.1:p.Glu44Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.833A>G
  hgvsp: ENSP00000455917.1:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.833A>G
  hgvsp: ENSP00000455724.1:p.Glu278Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.584A>G
  hgvsp: ENSP00000457514.1:p.Glu195Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.995A>G
  hgvsp: ENSP00000457468.2:p.Glu332Gly
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.337A>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu332Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-30081185-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081185
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081185
    reference: chr 16
allele count: 33
allele frequency: 2.728625764842071e-4
allele num: 120940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.834G>C
  hgvsp: ENSP00000336927.5:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.834G>C
  hgvsp: ENSP00000455724.1:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2028G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.338G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.996G>C
  hgvsp: ENSP00000457468.2:p.Glu332Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.846G>C
  hgvsp: ENSP00000378661.3:p.Glu282Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.834G>C
  hgvsp: ENSP00000455857.1:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.834G>C
  hgvsp: ENSP00000400452.2:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.834G>C
  hgvsp: ENSP00000455700.1:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.131G>C
  hgvsp: ENSP00000456098.1:p.Glu44Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.834G>C
  hgvsp: ENSP00000455917.1:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.996G>C
  hgvsp: ENSP00000378669.1:p.Glu332Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.834G>C
  hgvsp: ENSP00000455800.2:p.Glu278Asp
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.585G>C
  hgvsp: ENSP00000457514.1:p.Glu195Asp
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16969
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu332Asp
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

16-30081191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081191
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081191
    reference: chr 16
allele count: 7
allele frequency: 5.785602115877345e-5
allele num: 120990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.840G>A
  hgvsp: ENST00000569798.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.344G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.137G>A
  hgvsp: ENST00000565355.1:c.137G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.591G>A
  hgvsp: ENST00000564688.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1002G>A
  hgvsp: ENST00000395248.1:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.852G>A
  hgvsp: ENST00000395240.3:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.840G>A
  hgvsp: ENST00000569545.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1002G>A
  hgvsp: ENST00000564595.2:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.840G>A
  hgvsp: ENST00000412304.2:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2034G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.840G>A
  hgvsp: ENST00000563060.2:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.840G>A
  hgvsp: ENST00000564546.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.840G>A
  hgvsp: ENST00000338110.5:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.840G>A
  hgvsp: ENST00000566897.1:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala334Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-30081191-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081191
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081191
    reference: chr 16
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1002G>C
  hgvsp: ENST00000564595.2:c.1002G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.137G>C
  hgvsp: ENST00000565355.1:c.137G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1002G>C
  hgvsp: ENST00000395248.1:c.1002G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.840G>C
  hgvsp: ENST00000563060.2:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.840G>C
  hgvsp: ENST00000412304.2:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.840G>C
  hgvsp: ENST00000569545.1:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.852G>C
  hgvsp: ENST00000395240.3:c.852G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.840G>C
  hgvsp: ENST00000564546.1:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.591G>C
  hgvsp: ENST00000564688.1:c.591G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.344G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2034G>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.840G>C
  hgvsp: ENST00000338110.5:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.840G>C
  hgvsp: ENST00000566897.1:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.840G>C
  hgvsp: ENST00000569798.1:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala334Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-30081200-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081200
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081200
    reference: chr 16
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.353C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.849C>A
  hgvsp: ENSP00000455800.2:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.600C>A
  hgvsp: ENSP00000457514.1:p.Asn200Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.849C>A
  hgvsp: ENSP00000455700.1:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.146C>A
  hgvsp: ENSP00000456098.1:p.Asn49Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.849C>A
  hgvsp: ENSP00000455724.1:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.849C>A
  hgvsp: ENSP00000400452.2:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.849C>A
  hgvsp: ENSP00000455857.1:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2043C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.849C>A
  hgvsp: ENSP00000336927.5:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1011C>A
  hgvsp: ENSP00000457468.2:p.Asn337Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.861C>A
  hgvsp: ENSP00000378661.3:p.Asn287Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.849C>A
  hgvsp: ENSP00000455917.1:p.Asn283Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1011C>A
  hgvsp: ENSP00000378669.1:p.Asn337Lys
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn337Lys
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

16-30081200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081200
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081200
    reference: chr 16
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.849C>T
  hgvsp: ENST00000338110.5:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.861C>T
  hgvsp: ENST00000395240.3:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.849C>T
  hgvsp: ENST00000569545.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.849C>T
  hgvsp: ENST00000564546.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.849C>T
  hgvsp: ENST00000563060.2:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1011C>T
  hgvsp: ENST00000395248.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.849C>T
  hgvsp: ENST00000566897.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.849C>T
  hgvsp: ENST00000569798.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.849C>T
  hgvsp: ENST00000412304.2:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.146C>T
  hgvsp: ENST00000565355.1:c.146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.600C>T
  hgvsp: ENST00000564688.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.353C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1011C>T
  hgvsp: ENST00000564595.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2043C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17043
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn337Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

16-30081205-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081205
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081205
    reference: chr 16
allele count: 6
allele frequency: 4.959169504413661e-5
allele num: 120988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.854A>G
  hgvsp: ENSP00000400452.2:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.854A>G
  hgvsp: ENSP00000455724.1:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.854A>G
  hgvsp: ENSP00000455917.1:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.151A>G
  hgvsp: ENSP00000456098.1:p.Asn51Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2048A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1016A>G
  hgvsp: ENSP00000457468.2:p.Asn339Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.854A>G
  hgvsp: ENSP00000455857.1:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.866A>G
  hgvsp: ENSP00000378661.3:p.Asn289Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1016A>G
  hgvsp: ENSP00000378669.1:p.Asn339Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.854A>G
  hgvsp: ENSP00000455700.1:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.854A>G
  hgvsp: ENSP00000455800.2:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457514
  ensembl transcript: ENST00000564688
  gene symbol: ALDOA
  hgvsc: ENST00000564688.1:c.605A>G
  hgvsp: ENSP00000457514.1:p.Asn202Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.854A>G
  hgvsp: ENSP00000336927.5:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.358A>G
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8343
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn339Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-30081218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081218
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081218
    reference: chr 16
allele count: 2
allele frequency: 1.65404082172748e-5
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.867G>A
  hgvsp: ENST00000564546.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1029G>A
  hgvsp: ENST00000395248.1:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.879G>A
  hgvsp: ENST00000395240.3:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.867G>A
  hgvsp: ENST00000563060.2:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.867G>A
  hgvsp: ENST00000338110.5:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.867G>A
  hgvsp: ENST00000412304.2:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.867G>A
  hgvsp: ENST00000569545.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2061G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.867G>A
  hgvsp: ENST00000566897.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.164G>A
  hgvsp: ENST00000565355.1:c.164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1029G>A
  hgvsp: ENST00000564595.2:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.867G>A
  hgvsp: ENST00000569798.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.371G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys343Lys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

16-30081220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081220
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081220
    reference: chr 16
allele count: 2
allele frequency: 1.654478673769895e-5
allele num: 120884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1031G>A
  hgvsp: ENSP00000457468.2:p.Cys344Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.869G>A
  hgvsp: ENSP00000455700.1:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.373G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2063G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.869G>A
  hgvsp: ENSP00000455724.1:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.869G>A
  hgvsp: ENSP00000455917.1:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.881G>A
  hgvsp: ENSP00000378661.3:p.Cys294Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.869G>A
  hgvsp: ENSP00000336927.5:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.166G>A
  hgvsp: ENSP00000456098.1:p.Cys56Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.869G>A
  hgvsp: ENSP00000400452.2:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.869G>A
  hgvsp: ENSP00000455857.1:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1031G>A
  hgvsp: ENSP00000378669.1:p.Cys344Tyr
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.869G>A
  hgvsp: ENSP00000455800.2:p.Cys290Tyr
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17039
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys344Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-30081221-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081221
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081221
    reference: chr 16
allele count: 2
allele frequency: 1.654423929587718e-5
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.870C>T
  hgvsp: ENST00000412304.2:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.167C>T
  hgvsp: ENST00000565355.1:c.167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.374C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.870C>T
  hgvsp: ENST00000563060.2:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1032C>T
  hgvsp: ENST00000395248.1:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.882C>T
  hgvsp: ENST00000395240.3:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.870C>T
  hgvsp: ENST00000566897.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.870C>T
  hgvsp: ENST00000569545.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1032C>T
  hgvsp: ENST00000564595.2:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.870C>T
  hgvsp: ENST00000569798.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.870C>T
  hgvsp: ENST00000338110.5:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.870C>T
  hgvsp: ENST00000564546.1:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2064C>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys344Cys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-30081227-GCTGAAGCCCTGGGCCCTGACCTTCTCCTACGGCCGAGCCCTGCAGGCCTCTGCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081227
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081173
    reference: chr 16
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsp: ENSP00000378661.3:p.Pro299_Lys316del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsp: ENSP00000457468.2:p.Pro349_Lys366del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsp: ENSP00000456098.1:p.Pro61_Lys78del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsp: ENSP00000455724.1:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsp: ENSP00000455800.2:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsp: ENSP00000378669.1:p.Pro349_Lys366del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsp: ENSP00000455700.1:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsp: ENSP00000455857.1:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsp: ENSP00000336927.5:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsp: ENSP00000400452.2:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsp: ENSP00000455917.1:p.Pro295_Lys312del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro349_Lys366del
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: GCTGAAGCCCTGGGCCCTGACCTTCTCCTACGGCCGAGCCCTGCAGGCCTCTGCC
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

16-30081229-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081229
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081229
    reference: chr 16
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.175T>C
  hgvsp: ENSP00000456098.1:p.Leu59Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.878T>C
  hgvsp: ENSP00000336927.5:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.878T>C
  hgvsp: ENSP00000455724.1:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.878T>C
  hgvsp: ENSP00000455700.1:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1040T>C
  hgvsp: ENSP00000378669.1:p.Leu347Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.382T>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1040T>C
  hgvsp: ENSP00000457468.2:p.Leu347Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.878T>C
  hgvsp: ENSP00000400452.2:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.890T>C
  hgvsp: ENSP00000378661.3:p.Leu297Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.878T>C
  hgvsp: ENSP00000455800.2:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2072T>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.878T>C
  hgvsp: ENSP00000455857.1:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.878T>C
  hgvsp: ENSP00000455917.1:p.Leu293Pro
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu347Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

16-30081230-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081230
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081230
    reference: chr 16
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.891G>A
  hgvsp: ENST00000395240.3:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.879G>A
  hgvsp: ENST00000338110.5:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.383G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.879G>A
  hgvsp: ENST00000412304.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1041G>A
  hgvsp: ENST00000564595.2:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1041G>A
  hgvsp: ENST00000395248.1:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.879G>A
  hgvsp: ENST00000564546.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.176G>A
  hgvsp: ENST00000565355.1:c.176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.879G>A
  hgvsp: ENST00000569545.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.879G>A
  hgvsp: ENST00000569798.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.879G>A
  hgvsp: ENST00000563060.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2073G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.879G>A
  hgvsp: ENST00000566897.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16997
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu347Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-30081240-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081240
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081240
    reference: chr 16
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.393G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1051G>T
  hgvsp: ENSP00000457468.2:p.Ala351Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.889G>T
  hgvsp: ENSP00000455724.1:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.186G>T
  hgvsp: ENSP00000456098.1:p.Ala63Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2083G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.889G>T
  hgvsp: ENSP00000336927.5:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.901G>T
  hgvsp: ENSP00000378661.3:p.Ala301Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1051G>T
  hgvsp: ENSP00000378669.1:p.Ala351Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.889G>T
  hgvsp: ENSP00000455917.1:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.889G>T
  hgvsp: ENSP00000400452.2:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.889G>T
  hgvsp: ENSP00000455800.2:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.889G>T
  hgvsp: ENSP00000455700.1:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.889G>T
  hgvsp: ENSP00000455857.1:p.Ala297Ser
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala351Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-30081245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081245
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081245
    reference: chr 16
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.398G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.894G>A
  hgvsp: ENST00000412304.2:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.894G>A
  hgvsp: ENST00000563060.2:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1056G>A
  hgvsp: ENST00000564595.2:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1056G>A
  hgvsp: ENST00000395248.1:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.894G>A
  hgvsp: ENST00000569545.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.894G>A
  hgvsp: ENST00000338110.5:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.894G>A
  hgvsp: ENST00000564546.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.894G>A
  hgvsp: ENST00000569798.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.894G>A
  hgvsp: ENST00000566897.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.906G>A
  hgvsp: ENST00000395240.3:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.191G>A
  hgvsp: ENST00000565355.1:c.191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2088G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu352Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

16-30081250-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081250
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081247
    reference: chr 16
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1064_1066delCCT
  hgvsp: ENSP00000457468.2:p.Ser355del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.902_904delCCT
  hgvsp: ENSP00000400452.2:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.902_904delCCT
  hgvsp: ENSP00000455700.1:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.914_916delCCT
  hgvsp: ENSP00000378661.3:p.Ser305del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.902_904delCCT
  hgvsp: ENSP00000336927.5:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.902_904delCCT
  hgvsp: ENSP00000455800.2:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.199_201delCCT
  hgvsp: ENSP00000456098.1:p.Ser67del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.902_904delCCT
  hgvsp: ENSP00000455724.1:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.406_408delCCT
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.902_904delCCT
  hgvsp: ENSP00000455917.1:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1064_1066delCCT
  hgvsp: ENSP00000378669.1:p.Ser355del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.902_904delCCT
  hgvsp: ENSP00000455857.1:p.Ser301del
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2096_2098delCCT
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser355del
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: TCTC
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-30081256-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081256
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081256
    reference: chr 16
allele count: 1
allele frequency: 8.317391665973551e-6
allele num: 120230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.409A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.917A>C
  hgvsp: ENSP00000378661.3:p.Tyr306Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.905A>C
  hgvsp: ENSP00000455724.1:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.905A>C
  hgvsp: ENSP00000400452.2:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.905A>C
  hgvsp: ENSP00000455917.1:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1067A>C
  hgvsp: ENSP00000378669.1:p.Tyr356Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.905A>C
  hgvsp: ENSP00000455857.1:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.905A>C
  hgvsp: ENSP00000455700.1:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1067A>C
  hgvsp: ENSP00000457468.2:p.Tyr356Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.905A>C
  hgvsp: ENSP00000455800.2:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2099A>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.905A>C
  hgvsp: ENSP00000336927.5:p.Tyr302Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.202A>C
  hgvsp: ENSP00000456098.1:p.Tyr68Ser
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr356Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-30081257-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081257
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081257
    reference: chr 16
allele count: 24
allele frequency: 1.997403375611705e-4
allele num: 120156
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1068C>T
  hgvsp: ENST00000395248.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.906C>T
  hgvsp: ENST00000569545.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1068C>T
  hgvsp: ENST00000564595.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.906C>T
  hgvsp: ENST00000412304.2:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.906C>T
  hgvsp: ENST00000564546.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.906C>T
  hgvsp: ENST00000569798.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.918C>T
  hgvsp: ENST00000395240.3:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.203C>T
  hgvsp: ENST00000565355.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.906C>T
  hgvsp: ENST00000566897.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.410C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.906C>T
  hgvsp: ENST00000563060.2:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2100C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.906C>T
  hgvsp: ENST00000338110.5:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16555
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24451
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr356Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

16-30081258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081258
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081258
    reference: chr 16
allele count: 6
allele frequency: 4.992926687193143e-5
allele num: 120170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.907G>A
  hgvsp: ENSP00000455724.1:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1069G>A
  hgvsp: ENSP00000378669.1:p.Gly357Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.907G>A
  hgvsp: ENSP00000455700.1:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.907G>A
  hgvsp: ENSP00000400452.2:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.907G>A
  hgvsp: ENSP00000336927.5:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.907G>A
  hgvsp: ENSP00000455917.1:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.411G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1069G>A
  hgvsp: ENSP00000457468.2:p.Gly357Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.907G>A
  hgvsp: ENSP00000455857.1:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.919G>A
  hgvsp: ENSP00000378661.3:p.Gly307Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.907G>A
  hgvsp: ENSP00000455800.2:p.Gly303Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.204G>A
  hgvsp: ENSP00000456098.1:p.Gly69Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2101G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly357Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-30081269-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081269
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081269
    reference: chr 16
allele count: 1
allele frequency: 8.353521009105338e-6
allele num: 119710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.918G>A
  hgvsp: ENST00000569798.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.918G>A
  hgvsp: ENST00000566897.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.215G>A
  hgvsp: ENST00000565355.1:c.215G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1080G>A
  hgvsp: ENST00000395248.1:c.1080G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.918G>A
  hgvsp: ENST00000569545.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.918G>A
  hgvsp: ENST00000564546.1:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1080G>A
  hgvsp: ENST00000564595.2:c.1080G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.918G>A
  hgvsp: ENST00000412304.2:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.930G>A
  hgvsp: ENST00000395240.3:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2112G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.918G>A
  hgvsp: ENST00000338110.5:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.918G>A
  hgvsp: ENST00000563060.2:c.918G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.422G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu360Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

16-30081269-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081269
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081269
    reference: chr 16
allele count: 7
allele frequency: 5.847464706373737e-5
allele num: 119710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1080G>T
  hgvsp: ENST00000564595.2:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1080G>T
  hgvsp: ENST00000395248.1:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.918G>T
  hgvsp: ENST00000564546.1:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.422G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.930G>T
  hgvsp: ENST00000395240.3:c.930G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.918G>T
  hgvsp: ENST00000566897.1:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.918G>T
  hgvsp: ENST00000412304.2:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.918G>T
  hgvsp: ENST00000338110.5:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.918G>T
  hgvsp: ENST00000569798.1:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.918G>T
  hgvsp: ENST00000563060.2:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.918G>T
  hgvsp: ENST00000569545.1:c.918G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2112G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.215G>T
  hgvsp: ENST00000565355.1:c.215G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu360Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-30081280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081280
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081280
    reference: chr 16
allele count: 1
allele frequency: 8.367500627562547e-6
allele num: 119510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.226C>T
  hgvsp: ENSP00000456098.1:p.Ala76Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.929C>T
  hgvsp: ENSP00000400452.2:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.433C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1091C>T
  hgvsp: ENSP00000378669.1:p.Ala364Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.929C>T
  hgvsp: ENSP00000455724.1:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.929C>T
  hgvsp: ENSP00000455800.2:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.929C>T
  hgvsp: ENSP00000336927.5:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1091C>T
  hgvsp: ENSP00000457468.2:p.Ala364Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.941C>T
  hgvsp: ENSP00000378661.3:p.Ala314Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.929C>T
  hgvsp: ENSP00000455700.1:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2123C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.929C>T
  hgvsp: ENSP00000455917.1:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.929C>T
  hgvsp: ENSP00000455857.1:p.Ala310Val
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala364Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-30081293-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081293
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081293
    reference: chr 16
allele count: 2
allele frequency: 1.677880501350694e-5
allele num: 119198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.239G>T
  hgvsp: ENSP00000456098.1:p.Trp80Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1104G>T
  hgvsp: ENSP00000457468.2:p.Trp368Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2136G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.942G>T
  hgvsp: ENSP00000455857.1:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.942G>T
  hgvsp: ENSP00000455724.1:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.954G>T
  hgvsp: ENSP00000378661.3:p.Trp318Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.942G>T
  hgvsp: ENSP00000400452.2:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.942G>T
  hgvsp: ENSP00000455700.1:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1104G>T
  hgvsp: ENSP00000378669.1:p.Trp368Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.942G>T
  hgvsp: ENSP00000455800.2:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.942G>T
  hgvsp: ENSP00000455917.1:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.942G>T
  hgvsp: ENSP00000336927.5:p.Trp314Cys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.446G>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23931
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp368Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-30081296-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081296
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081296
    reference: chr 16
allele count: 9
allele frequency: 7.555279461392522e-5
allele num: 119122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.945C>T
  hgvsp: ENST00000569545.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.945C>T
  hgvsp: ENST00000412304.2:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.945C>T
  hgvsp: ENST00000569798.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.449C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2139C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.945C>T
  hgvsp: ENST00000564546.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.242C>T
  hgvsp: ENST00000565355.1:c.242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.957C>T
  hgvsp: ENST00000395240.3:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1107C>T
  hgvsp: ENST00000395248.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.945C>T
  hgvsp: ENST00000338110.5:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.945C>T
  hgvsp: ENST00000563060.2:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1107C>T
  hgvsp: ENST00000564595.2:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.945C>T
  hgvsp: ENST00000566897.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly369Gly
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-30081299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081299
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081299
    reference: chr 16
allele count: 1
allele frequency: 8.392218734789103e-6
allele num: 119158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.948G>A
  hgvsp: ENST00000566897.1:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.960G>A
  hgvsp: ENST00000395240.3:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.948G>A
  hgvsp: ENST00000569545.1:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.452G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1110G>A
  hgvsp: ENST00000395248.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.948G>A
  hgvsp: ENST00000563060.2:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.245G>A
  hgvsp: ENST00000565355.1:c.245G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1110G>A
  hgvsp: ENST00000564595.2:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.948G>A
  hgvsp: ENST00000569798.1:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.948G>A
  hgvsp: ENST00000338110.5:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.948G>A
  hgvsp: ENST00000412304.2:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2142G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.948G>A
  hgvsp: ENST00000564546.1:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23905
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly370Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-30081303-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081303
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081303
    reference: chr 16
allele count: 2
allele frequency: 1.678190239645566e-5
allele num: 119176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.952A>G
  hgvsp: ENSP00000400452.2:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2146A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.952A>G
  hgvsp: ENSP00000455700.1:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.952A>G
  hgvsp: ENSP00000455857.1:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1114A>G
  hgvsp: ENSP00000378669.1:p.Lys372Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1114A>G
  hgvsp: ENSP00000457468.2:p.Lys372Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.964A>G
  hgvsp: ENSP00000378661.3:p.Lys322Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.249A>G
  hgvsp: ENSP00000456098.1:p.Lys84Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.456A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.952A>G
  hgvsp: ENSP00000455724.1:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.952A>G
  hgvsp: ENSP00000455800.2:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.952A>G
  hgvsp: ENSP00000455917.1:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.952A>G
  hgvsp: ENSP00000336927.5:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16527
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys372Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-30081305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081305
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081305
    reference: chr 16
allele count: 1
allele frequency: 8.393768466290626e-6
allele num: 119136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.966G>A
  hgvsp: ENST00000395240.3:c.966G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1116G>A
  hgvsp: ENST00000395248.1:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.458G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.954G>A
  hgvsp: ENST00000412304.2:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.954G>A
  hgvsp: ENST00000338110.5:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.251G>A
  hgvsp: ENST00000565355.1:c.251G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.954G>A
  hgvsp: ENST00000569798.1:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.954G>A
  hgvsp: ENST00000563060.2:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1116G>A
  hgvsp: ENST00000564595.2:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.954G>A
  hgvsp: ENST00000569545.1:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2148G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.954G>A
  hgvsp: ENST00000564546.1:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.954G>A
  hgvsp: ENST00000566897.1:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys372Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-30081313-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081313
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081313
    reference: chr 16
allele count: 1
allele frequency: 8.406045628015669e-6
allele num: 118962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.962T>C
  hgvsp: ENSP00000455800.2:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.962T>C
  hgvsp: ENSP00000455700.1:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.974T>C
  hgvsp: ENSP00000378661.3:p.Leu325Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.962T>C
  hgvsp: ENSP00000455724.1:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1124T>C
  hgvsp: ENSP00000378669.1:p.Leu375Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.259T>C
  hgvsp: ENSP00000456098.1:p.Leu87Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1124T>C
  hgvsp: ENSP00000457468.2:p.Leu375Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.962T>C
  hgvsp: ENSP00000455857.1:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.962T>C
  hgvsp: ENSP00000336927.5:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.962T>C
  hgvsp: ENSP00000400452.2:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.466T>C
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.962T>C
  hgvsp: ENSP00000455917.1:p.Leu321Pro
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2156T>C
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu375Pro
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

16-30081314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081314
    reference: chr 16
allele count: 3
allele frequency: 2.52177129215561e-5
allele num: 118964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.260G>A
  hgvsp: ENST00000565355.1:c.260G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.963G>A
  hgvsp: ENST00000412304.2:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.467G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2157G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1125G>A
  hgvsp: ENST00000564595.2:c.1125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.963G>A
  hgvsp: ENST00000338110.5:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.963G>A
  hgvsp: ENST00000569798.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.963G>A
  hgvsp: ENST00000563060.2:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.963G>A
  hgvsp: ENST00000564546.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1125G>A
  hgvsp: ENST00000395248.1:c.1125G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.963G>A
  hgvsp: ENST00000569545.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.963G>A
  hgvsp: ENST00000566897.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.975G>A
  hgvsp: ENST00000395240.3:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8188
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu375Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-30081318-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081318
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081318
    reference: chr 16
allele count: 3
allele frequency: 2.521983287657414e-5
allele num: 118954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.264G>T
  hgvsp: ENSP00000456098.1:p.Ala89Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1129G>T
  hgvsp: ENSP00000378669.1:p.Ala377Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.967G>T
  hgvsp: ENSP00000455800.2:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.471G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.967G>T
  hgvsp: ENSP00000400452.2:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.967G>T
  hgvsp: ENSP00000455917.1:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.967G>T
  hgvsp: ENSP00000336927.5:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.967G>T
  hgvsp: ENSP00000455724.1:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.979G>T
  hgvsp: ENSP00000378661.3:p.Ala327Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.967G>T
  hgvsp: ENSP00000455700.1:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1129G>T
  hgvsp: ENSP00000457468.2:p.Ala377Ser
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2161G>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.967G>T
  hgvsp: ENSP00000455857.1:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23557
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala377Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

16-30081319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081319
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081319
    reference: chr 16
allele count: 1
allele frequency: 8.407883231317684e-6
allele num: 118936
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1130C>T
  hgvsp: ENSP00000378669.1:p.Ala377Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.968C>T
  hgvsp: ENSP00000455917.1:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.968C>T
  hgvsp: ENSP00000400452.2:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.968C>T
  hgvsp: ENSP00000455700.1:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.968C>T
  hgvsp: ENSP00000455857.1:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.968C>T
  hgvsp: ENSP00000455724.1:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1130C>T
  hgvsp: ENSP00000457468.2:p.Ala377Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.968C>T
  hgvsp: ENSP00000455800.2:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.980C>T
  hgvsp: ENSP00000378661.3:p.Ala327Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.472C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2162C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.265C>T
  hgvsp: ENSP00000456098.1:p.Ala89Val
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.968C>T
  hgvsp: ENSP00000336927.5:p.Ala323Val
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala377Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

16-30081323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081323
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081323
    reference: chr 16
allele count: 11
allele frequency: 9.253962378436585e-5
allele num: 118868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2166G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1134G>A
  hgvsp: ENST00000564595.2:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.972G>A
  hgvsp: ENST00000412304.2:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.972G>A
  hgvsp: ENST00000569545.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.269G>A
  hgvsp: ENST00000565355.1:c.269G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1134G>A
  hgvsp: ENST00000395248.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.984G>A
  hgvsp: ENST00000395240.3:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.972G>A
  hgvsp: ENST00000563060.2:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.972G>A
  hgvsp: ENST00000569798.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.972G>A
  hgvsp: ENST00000564546.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.972G>A
  hgvsp: ENST00000338110.5:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.972G>A
  hgvsp: ENST00000566897.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.476G>A
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16579
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala378Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

16-30081330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081330
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081330
    reference: chr 16
allele count: 2
allele frequency: 1.682736803136621e-5
allele num: 118854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.979G>A
  hgvsp: ENSP00000336927.5:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.979G>A
  hgvsp: ENSP00000400452.2:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.979G>A
  hgvsp: ENSP00000455917.1:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.979G>A
  hgvsp: ENSP00000455857.1:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.276G>A
  hgvsp: ENSP00000456098.1:p.Glu93Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1141G>A
  hgvsp: ENSP00000378669.1:p.Glu381Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.979G>A
  hgvsp: ENSP00000455700.1:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.991G>A
  hgvsp: ENSP00000378661.3:p.Glu331Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2173G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.979G>A
  hgvsp: ENSP00000455800.2:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1141G>A
  hgvsp: ENSP00000457468.2:p.Glu381Lys
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.483G>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.979G>A
  hgvsp: ENSP00000455724.1:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8205
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu381Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

16-30081340-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081340
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081340
    reference: chr 16
allele count: 5
allele frequency: 4.211022773211158e-5
allele num: 118736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.493A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.989A>G
  hgvsp: ENSP00000455700.1:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1151A>G
  hgvsp: ENSP00000378669.1:p.Lys384Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1151A>G
  hgvsp: ENSP00000457468.2:p.Lys384Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.989A>G
  hgvsp: ENSP00000455800.2:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2183A>G
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.989A>G
  hgvsp: ENSP00000400452.2:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.989A>G
  hgvsp: ENSP00000455857.1:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.989A>G
  hgvsp: ENSP00000455917.1:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.989A>G
  hgvsp: ENSP00000455724.1:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.286A>G
  hgvsp: ENSP00000456098.1:p.Lys96Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.1001A>G
  hgvsp: ENSP00000378661.3:p.Lys334Arg
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.989A>G
  hgvsp: ENSP00000336927.5:p.Lys330Arg
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys384Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

16-30081340-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081340
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081340
    reference: chr 16
allele count: 1
allele frequency: 8.422045546422314e-6
allele num: 118736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.286A>T
  hgvsp: ENSP00000456098.1:p.Lys96Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.989A>T
  hgvsp: ENSP00000336927.5:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.989A>T
  hgvsp: ENSP00000400452.2:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1151A>T
  hgvsp: ENSP00000457468.2:p.Lys384Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.989A>T
  hgvsp: ENSP00000455700.1:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.989A>T
  hgvsp: ENSP00000455857.1:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.989A>T
  hgvsp: ENSP00000455917.1:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.989A>T
  hgvsp: ENSP00000455800.2:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2183A>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1151A>T
  hgvsp: ENSP00000378669.1:p.Lys384Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.1001A>T
  hgvsp: ENSP00000378661.3:p.Lys334Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.989A>T
  hgvsp: ENSP00000455724.1:p.Lys330Met
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.493A>T
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16638
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys384Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-30081342-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081342
    reference: chr 16
allele count: 1
allele frequency: 8.427013634908062e-6
allele num: 118666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2185C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.991C>A
  hgvsp: ENST00000563060.2:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.991C>A
  hgvsp: ENST00000412304.2:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.991C>A
  hgvsp: ENST00000569798.1:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1153C>A
  hgvsp: ENST00000395248.1:c.1153C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.288C>A
  hgvsp: ENST00000565355.1:c.288C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.991C>A
  hgvsp: ENST00000338110.5:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.991C>A
  hgvsp: ENST00000569545.1:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.991C>A
  hgvsp: ENST00000564546.1:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.1003C>A
  hgvsp: ENST00000395240.3:c.1003C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.495C>A
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.991C>A
  hgvsp: ENST00000566897.1:c.991C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1153C>A
  hgvsp: ENST00000564595.2:c.1153C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg385Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-30081342-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081342
    reference: chr 16
allele count: 2
allele frequency: 1.685402726981612e-5
allele num: 118666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.495C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.991C>T
  hgvsp: ENSP00000400452.2:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.288C>T
  hgvsp: ENSP00000456098.1:p.Arg97Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1153C>T
  hgvsp: ENSP00000378669.1:p.Arg385Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2185C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.991C>T
  hgvsp: ENSP00000455857.1:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.991C>T
  hgvsp: ENSP00000455917.1:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.991C>T
  hgvsp: ENSP00000455800.2:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1153C>T
  hgvsp: ENSP00000457468.2:p.Arg385Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.991C>T
  hgvsp: ENSP00000455700.1:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.991C>T
  hgvsp: ENSP00000336927.5:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.991C>T
  hgvsp: ENSP00000455724.1:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.1003C>T
  hgvsp: ENSP00000378661.3:p.Arg335Ter
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg385Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

16-30081348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30081348
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 30081348
    reference: chr 16
allele count: 1
allele frequency: 8.427297702718647e-6
allele num: 118662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455917
  ensembl transcript: ENST00000564546
  gene symbol: ALDOA
  hgvsc: ENST00000564546.1:c.997C>T
  hgvsp: ENST00000564546.1:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378661
  ensembl transcript: ENST00000395240
  gene symbol: ALDOA
  hgvsc: ENST00000395240.3:c.1009C>T
  hgvsp: ENST00000395240.3:c.1009C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000566130
  gene symbol: ALDOA
  hgvsc: ENST00000566130.1:n.501C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000456098
  ensembl transcript: ENST00000565355
  gene symbol: ALDOA
  hgvsc: ENST00000565355.1:c.294C>T
  hgvsp: ENST00000565355.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455800
  ensembl transcript: ENST00000563060
  gene symbol: ALDOA
  hgvsc: ENST00000563060.2:c.997C>T
  hgvsp: ENST00000563060.2:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000378669
  ensembl transcript: ENST00000395248
  gene symbol: ALDOA
  hgvsc: ENST00000395248.1:c.1159C>T
  hgvsp: ENST00000395248.1:c.1159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455857
  ensembl transcript: ENST00000569798
  gene symbol: ALDOA
  hgvsc: ENST00000569798.1:c.997C>T
  hgvsp: ENST00000569798.1:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000457468
  ensembl transcript: ENST00000564595
  gene symbol: ALDOA
  hgvsc: ENST00000564595.2:c.1159C>T
  hgvsp: ENST00000564595.2:c.1159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455700
  ensembl transcript: ENST00000569545
  gene symbol: ALDOA
  hgvsc: ENST00000569545.1:c.997C>T
  hgvsp: ENST00000569545.1:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl transcript: ENST00000564521
  gene symbol: ALDOA
  hgvsc: ENST00000564521.2:n.2191C>T
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000400452
  ensembl transcript: ENST00000412304
  gene symbol: ALDOA
  hgvsc: ENST00000412304.2:c.997C>T
  hgvsp: ENST00000412304.2:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000336927
  ensembl transcript: ENST00000338110
  gene symbol: ALDOA
  hgvsc: ENST00000338110.5:c.997C>T
  hgvsp: ENST00000338110.5:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149925
  ensembl protein: ENSP00000455724
  ensembl transcript: ENST00000566897
  gene symbol: ALDOA
  hgvsc: ENST00000566897.1:c.997C>T
  hgvsp: ENST00000566897.1:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/414
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16744
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1159C>T
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1629
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5674
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5936
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 408
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4432
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3947
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12365
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.194251734390486e-5
allele num: 16144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.461e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

DP
type: SiteQuality
SIO_000300: 1.496511e6

FS
type: SiteQuality
SIO_000300: 8.195e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.13e1

GenotypeDepth
all individuals: 182
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5655
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10618
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2756
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 418
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4608
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4473
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5936
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3840
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.032520325203252e-4
allele num: 9840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

QD
type: SiteQuality
SIO_000300: 1.375e1

DP
type: SiteQuality
SIO_000300: 1.499973e6

FS
type: SiteQuality
SIO_000300: 4.398e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeDepth
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11423
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 176
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4473
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5936
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4608
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14299
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.016260162601626e-4
allele num: 9840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.183192742320547e-5
allele num: 62830
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 4.398e0

MQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

QD
type: SiteQuality
SIO_000300: 1.375e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.499973e6

GenotypeDepth
all individuals: 175
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 603
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2677
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4045
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4412
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5934
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.180863922641389e-5
allele num: 62876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10752
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.478e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
type: SiteQuality
SIO_000300: 1.504582e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 2.435e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

GenotypeDepth
all individuals: 5958
bin: 3.25e1
variant carriers: 9

GenotypeDepth
all individuals: 9191
bin: 1.75e1
variant carriers: 19

GenotypeDepth
all individuals: 1182
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 604
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2441
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4212
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3940
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4582
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5373
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2654
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6016
bin: 9.75e1
variant carriers: 90

GenotypeQuality
all individuals: 14916
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2416
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5772
num of homozygotes: 0

African
type: Population
allele count: 89
allele frequency: 9.03369874137231e-3
allele num: 9852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62998
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.849112426035503e-4
allele num: 10816
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 1.520863e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.993e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.194e0

QD
type: SiteQuality
SIO_000300: 1.457e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

GenotypeDepth
all individuals: 2809
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6106
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 842
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5939
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5731
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.5803280761086e-5
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InbreedingCoeff
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FS
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63248
num of homozygotes: 0

African
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South Asian
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allele frequency: 6.169031462060457e-5
allele num: 16210
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Latino
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East Asian
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European (Finnish)
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Other
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MQ
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FS
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
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allele num: 63748
num of homozygotes: 0

South Asian
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Other
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East Asian
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Latino
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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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

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

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

East Asian
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num of homozygotes: 0

Other
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65592
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Other
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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VQSLOD
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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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European (Non-Finnish)
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allele count: 22
allele frequency: 3.349675690489966e-4
allele num: 65678
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 1.514600751241973e-5
allele num: 66024
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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 frequency: 3.476245654692932e-4
allele num: 8630
num of homozygotes: 0

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

VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.925e1

FS
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SIO_000300: 9.409999999999999e-1

BaseQRankSum
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SIO_000300: 1.2e0

QD
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SIO_000300: 1.36e1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512721991952319e-5
allele num: 66106
num of homozygotes: 0

African
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allele frequency: 0.0e0
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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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DP
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VQSLOD
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MQRankSum
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FS
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8636
num of homozygotes: 0

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

South Asian
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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

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: 3
allele frequency: 4.531995890990392e-5
allele num: 66196
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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SIO_000300: -6.899999999999999e-1

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeDepth
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.549448890231014e-5
allele num: 66230
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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SIO_000300: -1.189e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.052504526252263e-5
allele num: 66280
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

BaseQRankSum
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SIO_000300: -2.033e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.093e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
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SIO_000300: 2.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.992e0

DP
type: SiteQuality
SIO_000300: 1.734719e6

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 8

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: 140

GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.057459328487366e-4
allele num: 11556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 65
allele frequency: 3.938916494970307e-3
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 65
allele frequency: 9.800078400627205e-4
allele num: 66326
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.283e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

BaseQRankSum
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SIO_000300: -7.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

VQSLOD
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SIO_000300: 3.89e0

DP
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SIO_000300: 1.743466e6

MQRankSum
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SIO_000300: 1.53e-1

MQ
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SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 9.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

BaseQRankSum
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SIO_000300: -3.521e0

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.505e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

QD
type: SiteQuality
SIO_000300: 7.38e0

DP
type: SiteQuality
SIO_000300: 1.733526e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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 count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.912e1

FS
type: SiteQuality
SIO_000300: 3.429e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

BaseQRankSum
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SIO_000300: -1.896e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 1.357e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.736103e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

East Asian
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allele count: 0
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allele num: 8642
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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QD
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VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

ClippingRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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allele frequency: 1.998788612961841e-3
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DP
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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South Asian
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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
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num of homozygotes: 0

African
type: Population
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allele frequency: 1.928640308582449e-4
allele num: 10370
num of homozygotes: 0

European (Finnish)
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allele count: 0
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East Asian
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European (Non-Finnish)
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FS
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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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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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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Other
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East Asian
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MQ
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FS
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QD
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQ
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DP
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QD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6576
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Latino
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East Asian
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European (Non-Finnish)
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African
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Other
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South Asian
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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Latino
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African
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European (Finnish)
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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VQSLOD
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FS
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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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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South Asian
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European (Finnish)
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Latino
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African
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East Asian
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQ
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DP
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BaseQRankSum
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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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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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East Asian
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BaseQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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DP
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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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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FS
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BaseQRankSum
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VQSLOD
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MQ
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MQRankSum
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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QD
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DP
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VQSLOD
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MQRankSum
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66066
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 6.2e-1

QD
type: SiteQuality
SIO_000300: 1.585e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.49e-1

DP
type: SiteQuality
SIO_000300: 1.722974e6

BaseQRankSum
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SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.776e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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
all individuals: 188
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516714190377965e-5
allele num: 65932
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
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SIO_000300: 1.718065e6

BaseQRankSum
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SIO_000300: 4.37e0

VQSLOD
type: SiteQuality
SIO_000300: 8.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

FS
type: SiteQuality
SIO_000300: 1.191e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.585e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
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SIO_000300: 1.371e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 24

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3532
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.187904180708625e-4
allele num: 65874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.887284951552304e-5
allele num: 10114
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.866e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.244e1

DP
type: SiteQuality
SIO_000300: 1.717485e6

VQSLOD
type: SiteQuality
SIO_000300: 3.21e-1

GenotypeDepth
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bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1749
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2535
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1202
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.198405822214521e-4
allele num: 11542
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.465e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 3.628e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 1.716992e6

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005025125628141e-4
allele num: 9950
num of homozygotes: 0

East Asian
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: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65608
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.711267e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

GenotypeDepth
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.240882103477523e-4
allele num: 16506
num of homozygotes: 0

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

Other
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
allele num: 8628
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.289e1

ReadPosRankSum
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VQSLOD
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DP
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FS
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MQ
type: SiteQuality
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527137228551358e-5
allele num: 65482
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South Asian
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QD
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FS
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ReadPosRankSum
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VQSLOD
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MQ
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DP
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MQRankSum
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BaseQRankSum
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SIO_000300: -3.912e0

ClippingRankSum
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SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65312
num of homozygotes: 0

Other
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East Asian
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South Asian
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European (Finnish)
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Latino
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DP
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FS
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.0275380189067e-4
allele num: 9732
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 3.064476587398872e-5
allele num: 65264
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East Asian
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MQRankSum
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FS
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BaseQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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South Asian
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FS
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DP
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BaseQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Finnish)
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East Asian
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Latino
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Other
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African
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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FS
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Other
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Latino
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European (Non-Finnish)
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South Asian
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African
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ReadPosRankSum
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MQRankSum
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DP
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FS
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MQ
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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East Asian
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1203
bin: 8.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.603203829865586e-5
allele num: 65172
num of homozygotes: 0

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

QD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 2.1e-3

ClippingRankSum
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MQ
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SIO_000300: 5.938e1

ReadPosRankSum
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SIO_000300: 4.87e-1

VQSLOD
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SIO_000300: 2.95e0

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.737e0

DP
type: SiteQuality
SIO_000300: 1.704413e6

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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variant carriers: 1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.098533360875852e-4
allele num: 9682
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65148
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQ
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SIO_000300: 5.959e1

ReadPosRankSum
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SIO_000300: -1.29e-1

DP
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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SIO_000300: 1.7e0

BaseQRankSum
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SIO_000300: -4.29e-1

GenotypeDepth
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65130
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
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SIO_000300: 1.704244e6

QD
type: SiteQuality
SIO_000300: 1.323e1

InbreedingCoeff
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SIO_000300: -5.0e-4

ClippingRankSum
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SIO_000300: 1.75e-1

BaseQRankSum
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SIO_000300: -3.919e0

FS
type: SiteQuality
SIO_000300: 8.292999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.608153359343799e-5
allele num: 65102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9656
num of homozygotes: 0

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

South Asian
type: Population
allele count: 8
allele frequency: 4.847309743092584e-4
allele num: 16504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.278e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.233e1

VQSLOD
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SIO_000300: 2.74e0

DP
type: SiteQuality
SIO_000300: 1.704475e6

InbreedingCoeff
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SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.073896471166851e-5
allele num: 65064
num of homozygotes: 0

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

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

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

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

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

Other
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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SIO_000300: 1.119e1

MQRankSum
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SIO_000300: 1.11e0

DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.036914143508917e-4
allele num: 9644
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 4.639294827186268e-4
allele num: 8622
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
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SIO_000300: 1.43e-1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

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

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

DP
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BaseQRankSum
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 2.445e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

GenotypeDepth
all individuals: 16617
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3136
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29617
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6042
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8122
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539882968894364e-5
allele num: 64940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 1.257e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 9.65e-1

DP
type: SiteQuality
SIO_000300: 1.704075e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

GenotypeDepth
all individuals: 1216
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8286
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8122
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2561
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6042
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29617
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.520218911523259e-4
allele num: 6578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539882968894364e-5
allele num: 64940
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.257e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.322e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.704075e6