10-6263678-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263678
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263678
    reference: chr 10
allele count: 1
allele frequency: 1.280409731113956e-5
allele num: 78100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1053C>T
  hgvsp: ENST00000467491.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1053C>T
  hgvsp: ENST00000477914.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1053C>T
  hgvsp: ENST00000379775.4:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1053C>T
  hgvsp: ENST00000461744.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1053C>T
  hgvsp: ENST00000379785.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+188C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.993C>T
  hgvsp: ENST00000379789.4:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1053C>T
  hgvsp: ENST00000490474.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1053C>T
  hgvsp: ENST00000360521.2:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+188C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1095C>T
  hgvsp: ENST00000540253.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1053C>T
  hgvsp: ENST00000379782.3:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1053C>T
  hgvsp: ENST00000317350.4:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp351Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

10-6263685-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263685
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263685
    reference: chr 10
allele count: 1
allele frequency: 1.35003780105843e-5
allele num: 74072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1060T>C
  hgvsp: ENSP00000369108.3:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1060T>C
  hgvsp: ENSP00000432356.1:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1060T>C
  hgvsp: ENSP00000369111.1:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+195T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1000T>C
  hgvsp: ENSP00000369115.4:p.Tyr334His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1060T>C
  hgvsp: ENSP00000436885.1:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1060T>C
  hgvsp: ENSP00000353712.2:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1060T>C
  hgvsp: ENSP00000434628.1:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1060T>C
  hgvsp: ENSP00000369100.4:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1060T>C
  hgvsp: ENSP00000433771.1:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1060T>C
  hgvsp: ENSP00000369105.3:p.Tyr354His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+195T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1102T>C
  hgvsp: ENSP00000446384.1:p.Tyr368His
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13999
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr354His
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

10-6263686-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263686
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263686
    reference: chr 10
allele count: 2
allele frequency: 2.702191477288081e-5
allele num: 74014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1061A>G
  hgvsp: ENSP00000432356.1:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+196A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1061A>G
  hgvsp: ENSP00000369100.4:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1103A>G
  hgvsp: ENSP00000446384.1:p.Tyr368Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1061A>G
  hgvsp: ENSP00000353712.2:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1001A>G
  hgvsp: ENSP00000369115.4:p.Tyr334Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1061A>G
  hgvsp: ENSP00000369105.3:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1061A>G
  hgvsp: ENSP00000434628.1:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1061A>G
  hgvsp: ENSP00000436885.1:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1061A>G
  hgvsp: ENSP00000433771.1:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+196A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1061A>G
  hgvsp: ENSP00000369108.3:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1061A>G
  hgvsp: ENSP00000369111.1:p.Tyr354Cys
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19788
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr354Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

10-6263692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263692
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263692
    reference: chr 10
allele count: 1
allele frequency: 1.423203916657179e-5
allele num: 70264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1067G>A
  hgvsp: ENSP00000369111.1:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1007G>A
  hgvsp: ENSP00000369115.4:p.Arg336His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1067G>A
  hgvsp: ENSP00000432356.1:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1067G>A
  hgvsp: ENSP00000369105.3:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1109G>A
  hgvsp: ENSP00000446384.1:p.Arg370His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1067G>A
  hgvsp: ENSP00000353712.2:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1067G>A
  hgvsp: ENSP00000434628.1:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1067G>A
  hgvsp: ENSP00000369100.4:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1067G>A
  hgvsp: ENSP00000433771.1:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+202G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+202G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1067G>A
  hgvsp: ENSP00000369108.3:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1067G>A
  hgvsp: ENSP00000436885.1:p.Arg356His
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20408
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15030
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg356His
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

10-6263702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263702
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263702
    reference: chr 10
allele count: 5
allele frequency: 7.890168849613381e-5
allele num: 63370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1077C>T
  hgvsp: ENST00000467491.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1077C>T
  hgvsp: ENST00000317350.4:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1077C>T
  hgvsp: ENST00000379782.3:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1077C>T
  hgvsp: ENST00000461744.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1077C>T
  hgvsp: ENST00000379785.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1077C>T
  hgvsp: ENST00000477914.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1077C>T
  hgvsp: ENST00000360521.2:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1119C>T
  hgvsp: ENST00000540253.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+212C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1077C>T
  hgvsp: ENST00000490474.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1017C>T
  hgvsp: ENST00000379789.4:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+212C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1077C>T
  hgvsp: ENST00000379775.4:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15986
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21305
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr359Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

10-6263703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263703
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263703
    reference: chr 10
allele count: 1
allele frequency: 1.612487100103199e-5
allele num: 62016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1078G>A
  hgvsp: ENSP00000432356.1:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1018G>A
  hgvsp: ENSP00000369115.4:p.Gly340Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+213G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1078G>A
  hgvsp: ENSP00000369108.3:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1078G>A
  hgvsp: ENSP00000433771.1:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1078G>A
  hgvsp: ENSP00000369111.1:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1078G>A
  hgvsp: ENSP00000436885.1:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1078G>A
  hgvsp: ENSP00000434628.1:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1120G>A
  hgvsp: ENSP00000446384.1:p.Gly374Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1078G>A
  hgvsp: ENSP00000369105.3:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+213G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1078G>A
  hgvsp: ENSP00000353712.2:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1078G>A
  hgvsp: ENSP00000369100.4:p.Gly360Arg
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly360Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-6263705-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263705
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263705
    reference: chr 10
allele count: 1
allele frequency: 1.645982157553412e-5
allele num: 60754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1080G>T
  hgvsp: ENST00000477914.1:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1080G>T
  hgvsp: ENST00000461744.1:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1122G>T
  hgvsp: ENST00000540253.1:c.1122G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1080G>T
  hgvsp: ENST00000379785.1:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1080G>T
  hgvsp: ENST00000379782.3:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1080G>T
  hgvsp: ENST00000467491.1:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1080G>T
  hgvsp: ENST00000379775.4:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+215G>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1080G>T
  hgvsp: ENST00000360521.2:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1020G>T
  hgvsp: ENST00000379789.4:c.1020G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1080G>T
  hgvsp: ENST00000317350.4:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+215G>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1080G>T
  hgvsp: ENST00000490474.1:c.1080G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly360Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS

10-6263714-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263714
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263714
    reference: chr 10
allele count: 17
allele frequency: 3.081273109548321e-4
allele num: 55172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+224C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+224C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+6C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21188
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1083+6C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

10-6263715-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263715
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263715
    reference: chr 10
allele count: 1
allele frequency: 1.92596587188475e-5
allele num: 51922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+225G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+7G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+225G>C
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15870
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1083+7G>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

10-6263726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263726
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263726
    reference: chr 10
allele count: 2
allele frequency: 4.87757291971515e-5
allele num: 41004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+18C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+236C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+236C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-6263727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263727
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263727
    reference: chr 10
allele count: 2
allele frequency: 4.877097151775263e-5
allele num: 41008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+237G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+237G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+19G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21119
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-6263729-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263729
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263729
    reference: chr 10
allele count: 1
allele frequency: 2.527039320731831e-5
allele num: 39572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+239G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+239G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+21G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+21G>C
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18022
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

10-6263733-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263733
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263733
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 36722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+243A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+243A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+25A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+25A>G
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21148
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

10-6263734-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263734
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263734
    reference: chr 10
allele count: 10
allele frequency: 2.846407833314358e-4
allele num: 35132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+244C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+244C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+26C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+26C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10933
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

10-6263735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263735
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263735
    reference: chr 10
allele count: 6
allele frequency: 1.714187760699389e-4
allele num: 35002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+245G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+245G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+27G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21297
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

10-6263741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263741
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263741
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 32666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+251C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+251C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+33C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+33C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21354
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

10-6263747-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263747
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263747
    reference: chr 10
allele count: 11
allele frequency: 3.593831677992681e-4
allele num: 30608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+257A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+257A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+39A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+39A>G
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21833
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21331
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: A
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

10-6263749-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263749
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263749
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 30126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+259A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+259A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+41A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+41A>G
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22031
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

10-6263749-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6263749
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6263749
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 30126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1125+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.124+259A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1023+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*413+259A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1083+41A>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22031
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

10-6264767-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264767
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264767
    reference: chr 10
allele count: 1
allele frequency: 9.572125969177754e-6
allele num: 104470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1154A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.97A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-51A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-51A>G
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12739
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-6264769-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264769
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264769
    reference: chr 10
allele count: 1
allele frequency: 9.625194910196932e-6
allele num: 103894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.99C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1152C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-49C>A
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-6264775-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264775
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264775
    reference: chr 10
allele count: 2
allele frequency: 1.913655848132272e-5
allele num: 104512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.105C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1146C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-43C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-43C>G
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

10-6264776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264776
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264776
    reference: chr 10
allele count: 5
allele frequency: 4.794047710362814e-5
allele num: 104296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1145C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.106C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-42C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-42C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11540
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16878
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-6264777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264777
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264777
    reference: chr 10
allele count: 14
allele frequency: 1.33945656333716e-4
allele num: 104520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.107G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1144G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-41G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7301
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10716
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13746
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

10-6264778-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264778
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264778
    reference: chr 10
allele count: 1
allele frequency: 9.52580540684715e-6
allele num: 104978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.108A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-40A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1143A>G
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9751
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

10-6264788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264788
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264788
    reference: chr 10
allele count: 1
allele frequency: 9.429158730458069e-6
allele num: 106054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1133G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.118G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-30G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-30G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24664
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

10-6264791-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264791
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264791
    reference: chr 10
allele count: 2
allele frequency: 1.878569281635107e-5
allele num: 106464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.121C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1130C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-27C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-27C>G
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25842
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

10-6264793-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264793
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264793
    reference: chr 10
allele count: 25
allele frequency: 2.343676760101247e-4
allele num: 106670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.123C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-25C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1128C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6670
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26834
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

10-6264794-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264794
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264794
    reference: chr 10
allele count: 3
allele frequency: 2.800963531454821e-5
allele num: 107106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1127G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.124G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-24G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-24G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27843
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

10-6264801-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264801
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264801
    reference: chr 10
allele count: 4
allele frequency: 3.686432086704882e-5
allele num: 108506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1120C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.131C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-17C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-17C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29558
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

10-6264802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264802
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264802
    reference: chr 10
allele count: 2
allele frequency: 1.834424816098912e-5
allele num: 109026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1119G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.132G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-16G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-16G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29857
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10863
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

10-6264803-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264803
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264803
    reference: chr 10
allele count: 2
allele frequency: 1.830127559890924e-5
allele num: 109282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1118G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.133G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-15G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-6264816-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264816
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264816
    reference: chr 10
allele count: 1
allele frequency: 8.893157604539068e-6
allele num: 112446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1024-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1105A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.146A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1126-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1084-2A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.125-2A>G
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1084-2A>G
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP

10-6264829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264829
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264829
    reference: chr 10
allele count: 1
allele frequency: 8.696105883785241e-6
allele num: 114994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1095C>T
  hgvsp: ENST00000379782.3:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1092C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1095C>T
  hgvsp: ENST00000461744.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1095C>T
  hgvsp: ENST00000379785.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1095C>T
  hgvsp: ENST00000467491.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1137C>T
  hgvsp: ENST00000540253.1:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1095C>T
  hgvsp: ENST00000379775.4:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.159C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1095C>T
  hgvsp: ENST00000317350.4:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1095C>T
  hgvsp: ENST00000477914.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1095C>T
  hgvsp: ENST00000360521.2:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1095C>T
  hgvsp: ENST00000490474.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.136C>T
  hgvsp: ENST00000450232.1:c.136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1035C>T
  hgvsp: ENST00000379789.4:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp365Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-6264832-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264832
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264832
    reference: chr 10
allele count: 1
allele frequency: 8.662508662508662e-6
allele num: 115440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1038G>C
  hgvsp: ENST00000379789.4:c.1038G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1140G>C
  hgvsp: ENST00000540253.1:c.1140G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1098G>C
  hgvsp: ENST00000467491.1:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1098G>C
  hgvsp: ENST00000379785.1:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1098G>C
  hgvsp: ENST00000477914.1:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1098G>C
  hgvsp: ENST00000379782.3:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.139G>C
  hgvsp: ENST00000450232.1:c.139G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1098G>C
  hgvsp: ENST00000317350.4:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1098G>C
  hgvsp: ENST00000379775.4:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1089G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1098G>C
  hgvsp: ENST00000490474.1:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1098G>C
  hgvsp: ENST00000461744.1:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1098G>C
  hgvsp: ENST00000360521.2:c.1098G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.162G>C
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu366Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

10-6264839-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264839
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264839
    reference: chr 10
allele count: 4
allele frequency: 3.441629955947137e-5
allele num: 116224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1105C>T
  hgvsp: ENSP00000369111.1:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1105C>T
  hgvsp: ENSP00000369108.3:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1105C>T
  hgvsp: ENSP00000369100.4:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1105C>T
  hgvsp: ENSP00000353712.2:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1105C>T
  hgvsp: ENSP00000432356.1:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.146C>T
  hgvsp: ENSP00000390285.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1105C>T
  hgvsp: ENSP00000436885.1:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1105C>T
  hgvsp: ENSP00000434628.1:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.169C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1105C>T
  hgvsp: ENSP00000369105.3:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1147C>T
  hgvsp: ENSP00000446384.1:p.Arg383Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1045C>T
  hgvsp: ENSP00000369115.4:p.Arg349Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1105C>T
  hgvsp: ENSP00000433771.1:p.Arg369Cys
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1082C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg369Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

10-6264844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264844
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264844
    reference: chr 10
allele count: 1
allele frequency: 8.554612647139337e-6
allele num: 116896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.174G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1110G>A
  hgvsp: ENST00000379775.4:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1110G>A
  hgvsp: ENST00000379785.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.151G>A
  hgvsp: ENST00000450232.1:c.151G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1110G>A
  hgvsp: ENST00000477914.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1152G>A
  hgvsp: ENST00000540253.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1110G>A
  hgvsp: ENST00000461744.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1110G>A
  hgvsp: ENST00000379782.3:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1110G>A
  hgvsp: ENST00000490474.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1110G>A
  hgvsp: ENST00000317350.4:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1110G>A
  hgvsp: ENST00000467491.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1110G>A
  hgvsp: ENST00000360521.2:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1050G>A
  hgvsp: ENST00000379789.4:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1077G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu370Leu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

10-6264847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264847
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264847
    reference: chr 10
allele count: 13
allele frequency: 1.109953723467837e-4
allele num: 117122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1053G>A
  hgvsp: ENST00000379789.4:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1113G>A
  hgvsp: ENST00000379775.4:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1113G>A
  hgvsp: ENST00000360521.2:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1113G>A
  hgvsp: ENST00000379785.1:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1074G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1155G>A
  hgvsp: ENST00000540253.1:c.1155G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.154G>A
  hgvsp: ENST00000450232.1:c.154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1113G>A
  hgvsp: ENST00000477914.1:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.177G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1113G>A
  hgvsp: ENST00000379782.3:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1113G>A
  hgvsp: ENST00000317350.4:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1113G>A
  hgvsp: ENST00000467491.1:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1113G>A
  hgvsp: ENST00000461744.1:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1113G>A
  hgvsp: ENST00000490474.1:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu371Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

10-6264848-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264848
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264848
    reference: chr 10
allele count: 1
allele frequency: 8.536502082906508e-6
allele num: 117144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1114C>G
  hgvsp: ENSP00000369108.3:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1114C>G
  hgvsp: ENSP00000353712.2:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1114C>G
  hgvsp: ENSP00000433771.1:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1114C>G
  hgvsp: ENSP00000432356.1:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1114C>G
  hgvsp: ENSP00000434628.1:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1073C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1156C>G
  hgvsp: ENSP00000446384.1:p.Pro386Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.155C>G
  hgvsp: ENSP00000390285.1:p.Pro53Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1114C>G
  hgvsp: ENSP00000436885.1:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1114C>G
  hgvsp: ENSP00000369100.4:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1114C>G
  hgvsp: ENSP00000369105.3:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.178C>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1054C>G
  hgvsp: ENSP00000369115.4:p.Pro352Ala
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1114C>G
  hgvsp: ENSP00000369111.1:p.Pro372Ala
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro372Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-6264856-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264856
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264856
    reference: chr 10
allele count: 4
allele frequency: 3.40901343151292e-5
allele num: 117336
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1122C>A
  hgvsp: ENST00000379775.4:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1122C>A
  hgvsp: ENST00000317350.4:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1122C>A
  hgvsp: ENST00000461744.1:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1122C>A
  hgvsp: ENST00000379785.1:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1122C>A
  hgvsp: ENST00000379782.3:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.163C>A
  hgvsp: ENST00000450232.1:c.163C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1122C>A
  hgvsp: ENST00000467491.1:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.186C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1164C>A
  hgvsp: ENST00000540253.1:c.1164C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1122C>A
  hgvsp: ENST00000360521.2:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1062C>A
  hgvsp: ENST00000379789.4:c.1062C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1065C>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1122C>A
  hgvsp: ENST00000490474.1:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1122C>A
  hgvsp: ENST00000477914.1:c.1122C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35063
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile374Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

10-6264856-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264856
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264856
    reference: chr 10
allele count: 1
allele frequency: 8.522533578782301e-6
allele num: 117336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1122C>T
  hgvsp: ENST00000461744.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.163C>T
  hgvsp: ENST00000450232.1:c.163C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1122C>T
  hgvsp: ENST00000379782.3:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1065C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1122C>T
  hgvsp: ENST00000360521.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1122C>T
  hgvsp: ENST00000477914.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1122C>T
  hgvsp: ENST00000490474.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1062C>T
  hgvsp: ENST00000379789.4:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.186C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1122C>T
  hgvsp: ENST00000467491.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1122C>T
  hgvsp: ENST00000379775.4:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1122C>T
  hgvsp: ENST00000317350.4:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1122C>T
  hgvsp: ENST00000379785.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1164C>T
  hgvsp: ENST00000540253.1:c.1164C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile374Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

10-6264870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264870
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264870
    reference: chr 10
allele count: 1
allele frequency: 8.543649505322693e-6
allele num: 117046
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1136G>A
  hgvsp: ENSP00000369100.4:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1136G>A
  hgvsp: ENSP00000432356.1:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1136G>A
  hgvsp: ENSP00000353712.2:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1136G>A
  hgvsp: ENSP00000433771.1:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1136G>A
  hgvsp: ENSP00000369105.3:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1178G>A
  hgvsp: ENSP00000446384.1:p.Arg393Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1076G>A
  hgvsp: ENSP00000369115.4:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1136G>A
  hgvsp: ENSP00000434628.1:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1136G>A
  hgvsp: ENSP00000436885.1:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.177G>A
  hgvsp: ENSP00000390285.1:p.Arg60Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1136G>A
  hgvsp: ENSP00000369111.1:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1136G>A
  hgvsp: ENSP00000369108.3:p.Arg379Gln
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1051G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.200G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg379Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

10-6264876-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264876
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264876
    reference: chr 10
allele count: 102
allele frequency: 8.986150755893857e-4
allele num: 113508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1142A>G
  hgvsp: ENSP00000434628.1:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1142A>G
  hgvsp: ENSP00000436885.1:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1142A>G
  hgvsp: ENSP00000432356.1:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1142A>G
  hgvsp: ENSP00000433771.1:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1142A>G
  hgvsp: ENSP00000369108.3:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.183A>G
  hgvsp: ENSP00000390285.1:p.Glu62Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1142A>G
  hgvsp: ENSP00000369105.3:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1184A>G
  hgvsp: ENSP00000446384.1:p.Glu395Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.206A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1142A>G
  hgvsp: ENSP00000369100.4:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1142A>G
  hgvsp: ENSP00000353712.2:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1045A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1142A>G
  hgvsp: ENSP00000369111.1:p.Glu381Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1082A>G
  hgvsp: ENSP00000369115.4:p.Glu361Gly
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 15682
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu381Gly
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-6264883-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264883
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264883
    reference: chr 10
allele count: 3062
allele frequency: 2.61879511477541e-2
allele num: 116924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1191G>A
  hgvsp: ENST00000540253.1:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1149G>A
  hgvsp: ENST00000379782.3:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1149G>A
  hgvsp: ENST00000360521.2:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1149G>A
  hgvsp: ENST00000467491.1:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1149G>A
  hgvsp: ENST00000461744.1:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1149G>A
  hgvsp: ENST00000490474.1:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1149G>A
  hgvsp: ENST00000477914.1:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1149G>A
  hgvsp: ENST00000317350.4:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1038G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1089G>A
  hgvsp: ENST00000379789.4:c.1089G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.213G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1149G>A
  hgvsp: ENST00000379775.4:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.190G>A
  hgvsp: ENST00000450232.1:c.190G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1149G>A
  hgvsp: ENST00000379785.1:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.25e1
  variant carriers: 345
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 1.25e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 31528
  bin: 2.25e1
  variant carriers: 377
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.75e1
  variant carriers: 326
genotype quality: GenotypeQuality
hgvs: p.Val383Val
num of homozygotes: 339
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

10-6264901-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264901
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264901
    reference: chr 10
allele count: 2
allele frequency: 1.723454492184134e-5
allele num: 116046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1209G>A
  hgvsp: ENST00000540253.1:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1167G>A
  hgvsp: ENST00000317350.4:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1167G>A
  hgvsp: ENST00000360521.2:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.208G>A
  hgvsp: ENST00000450232.1:c.208G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1167G>A
  hgvsp: ENST00000379785.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1167G>A
  hgvsp: ENST00000477914.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1020G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.231G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1107G>A
  hgvsp: ENST00000379789.4:c.1107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1167G>A
  hgvsp: ENST00000490474.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1167G>A
  hgvsp: ENST00000461744.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1167G>A
  hgvsp: ENST00000379775.4:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1167G>A
  hgvsp: ENST00000467491.1:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1167G>A
  hgvsp: ENST00000379782.3:c.1167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln389Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

10-6264904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264904
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264904
    reference: chr 10
allele count: 1
allele frequency: 8.63453468492583e-6
allele num: 115814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1170C>T
  hgvsp: ENST00000360521.2:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1170C>T
  hgvsp: ENST00000467491.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.234C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1017C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1110C>T
  hgvsp: ENST00000379789.4:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.211C>T
  hgvsp: ENST00000450232.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1170C>T
  hgvsp: ENST00000379775.4:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1170C>T
  hgvsp: ENST00000477914.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1170C>T
  hgvsp: ENST00000379785.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1170C>T
  hgvsp: ENST00000317350.4:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1212C>T
  hgvsp: ENST00000540253.1:c.1212C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1170C>T
  hgvsp: ENST00000490474.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1170C>T
  hgvsp: ENST00000379782.3:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1170C>T
  hgvsp: ENST00000461744.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala390Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

10-6264905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264905
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264905
    reference: chr 10
allele count: 1
allele frequency: 8.645732466454558e-6
allele num: 115664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.235G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1171G>A
  hgvsp: ENSP00000369108.3:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1171G>A
  hgvsp: ENSP00000433771.1:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1111G>A
  hgvsp: ENSP00000369115.4:p.Val371Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.212G>A
  hgvsp: ENSP00000390285.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1213G>A
  hgvsp: ENSP00000446384.1:p.Val405Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1171G>A
  hgvsp: ENSP00000369105.3:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1171G>A
  hgvsp: ENSP00000369111.1:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1171G>A
  hgvsp: ENSP00000434628.1:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1171G>A
  hgvsp: ENSP00000353712.2:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1171G>A
  hgvsp: ENSP00000436885.1:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1171G>A
  hgvsp: ENSP00000369100.4:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1016G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1171G>A
  hgvsp: ENSP00000432356.1:p.Val391Ile
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val391Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-6264910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264910
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264910
    reference: chr 10
allele count: 1
allele frequency: 8.659658116697553e-6
allele num: 115478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.217G>A
  hgvsp: ENST00000450232.1:c.217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1176G>A
  hgvsp: ENST00000477914.1:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1176G>A
  hgvsp: ENST00000360521.2:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1176G>A
  hgvsp: ENST00000317350.4:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1176G>A
  hgvsp: ENST00000379785.1:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1116G>A
  hgvsp: ENST00000379789.4:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1218G>A
  hgvsp: ENST00000540253.1:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1176G>A
  hgvsp: ENST00000461744.1:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1176G>A
  hgvsp: ENST00000467491.1:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1176G>A
  hgvsp: ENST00000379775.4:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.240G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1176G>A
  hgvsp: ENST00000490474.1:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1176G>A
  hgvsp: ENST00000379782.3:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1011G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu392Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

10-6264912-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264912
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264912
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 115308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1178G>T
  hgvsp: ENSP00000436885.1:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1178G>T
  hgvsp: ENSP00000353712.2:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.242G>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1178G>T
  hgvsp: ENSP00000369108.3:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1118G>T
  hgvsp: ENSP00000369115.4:p.Arg373Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1009G>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1178G>T
  hgvsp: ENSP00000369100.4:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1178G>T
  hgvsp: ENSP00000433771.1:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1178G>T
  hgvsp: ENSP00000369111.1:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1178G>T
  hgvsp: ENSP00000432356.1:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1220G>T
  hgvsp: ENSP00000446384.1:p.Arg407Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1178G>T
  hgvsp: ENSP00000434628.1:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1178G>T
  hgvsp: ENSP00000369105.3:p.Arg393Leu
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.219G>T
  hgvsp: ENSP00000390285.1:p.Arg74Leu
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg393Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

10-6264920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264920
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264920
    reference: chr 10
allele count: 1
allele frequency: 8.695198511382016e-6
allele num: 115006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1186C>T
  hgvsp: ENSP00000369111.1:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1228C>T
  hgvsp: ENSP00000446384.1:p.Leu410Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1186C>T
  hgvsp: ENSP00000369105.3:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1186C>T
  hgvsp: ENSP00000432356.1:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1186C>T
  hgvsp: ENSP00000353712.2:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.227C>T
  hgvsp: ENSP00000390285.1:p.Leu77Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1186C>T
  hgvsp: ENSP00000369100.4:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1186C>T
  hgvsp: ENSP00000434628.1:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.250C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1186C>T
  hgvsp: ENSP00000436885.1:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1186C>T
  hgvsp: ENSP00000433771.1:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1126C>T
  hgvsp: ENSP00000369115.4:p.Leu376Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1186C>T
  hgvsp: ENSP00000369108.3:p.Leu396Phe
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-1001C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu396Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-6264936-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264936
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264936
    reference: chr 10
allele count: 3
allele frequency: 2.640380214750924e-5
allele num: 113620
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1202A>T
  hgvsp: ENSP00000369100.4:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1202A>T
  hgvsp: ENSP00000434628.1:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1202A>T
  hgvsp: ENSP00000432356.1:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1202A>T
  hgvsp: ENSP00000436885.1:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.266A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1202A>T
  hgvsp: ENSP00000353712.2:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1202A>T
  hgvsp: ENSP00000369105.3:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.243A>T
  hgvsp: ENSP00000390285.1:p.Asp82Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-985A>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1142A>T
  hgvsp: ENSP00000369115.4:p.Asp381Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1244A>T
  hgvsp: ENSP00000446384.1:p.Asp415Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1202A>T
  hgvsp: ENSP00000369111.1:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1202A>T
  hgvsp: ENSP00000433771.1:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1202A>T
  hgvsp: ENSP00000369108.3:p.Asp401Val
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp401Val
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

10-6264941-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264941
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264941
    reference: chr 10
allele count: 2
allele frequency: 1.770036816765789e-5
allele num: 112992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1207A>G
  hgvsp: ENSP00000353712.2:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1147A>G
  hgvsp: ENSP00000369115.4:p.Ser383Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.248A>G
  hgvsp: ENSP00000390285.1:p.Ser84Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1207A>G
  hgvsp: ENSP00000434628.1:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1249A>G
  hgvsp: ENSP00000446384.1:p.Ser417Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1207A>G
  hgvsp: ENSP00000433771.1:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-980A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1207A>G
  hgvsp: ENSP00000369105.3:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1207A>G
  hgvsp: ENSP00000369100.4:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1207A>G
  hgvsp: ENSP00000432356.1:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1207A>G
  hgvsp: ENSP00000436885.1:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.271A>G
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1207A>G
  hgvsp: ENSP00000369108.3:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1207A>G
  hgvsp: ENSP00000369111.1:p.Ser403Gly
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser403Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

10-6264954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264954
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264954
    reference: chr 10
allele count: 5
allele frequency: 4.548348949331393e-5
allele num: 109930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-967C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+7C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+7C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1213+7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

10-6264955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264955
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264955
    reference: chr 10
allele count: 267
allele frequency: 2.429569775060057e-3
allele num: 109896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-966G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+8G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+8G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10509
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14205
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 3.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: c.1213+8G>A
num of homozygotes: 2
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-6264955-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264955
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264955
    reference: chr 10
allele count: 1
allele frequency: 9.099512266142535e-6
allele num: 109896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+8G>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-966G>C
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1213+8G>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

10-6264962-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264962
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264962
    reference: chr 10
allele count: 1
allele frequency: 9.205729646131752e-6
allele num: 108628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-959T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+15T>C
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+15T>C
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

10-6264963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264963
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264963
    reference: chr 10
allele count: 4
allele frequency: 3.698019710445057e-5
allele num: 108166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-958C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+16C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+16C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

10-6264966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264966
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264966
    reference: chr 10
allele count: 621
allele frequency: 5.76120233787921e-3
allele num: 107790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-955G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+19G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+19G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 2.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 1.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 18387
  bin: 2.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 3.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 3
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

10-6264968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264968
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264968
    reference: chr 10
allele count: 14
allele frequency: 1.306482017208234e-4
allele num: 107158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-953C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+21C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+21C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17386
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16706
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP

10-6264971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264971
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264971
    reference: chr 10
allele count: 62
allele frequency: 5.835294117647058e-4
allele num: 106250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-950C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+24C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+24C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-6264971-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264971
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264970
    reference: chr 10
allele count: 1
allele frequency: 9.411764705882352e-6
allele num: 106250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-947delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+27delG
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+27delG
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18293
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: CG
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-6264972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264972
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264972
    reference: chr 10
allele count: 11
allele frequency: 1.03948139328306e-4
allele num: 105822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-949G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+25G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+25G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13843
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

10-6264988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264988
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264988
    reference: chr 10
allele count: 1
allele frequency: 9.844457570387871e-6
allele num: 101580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-933G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+41G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+41G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

10-6264989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264989
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264989
    reference: chr 10
allele count: 1
allele frequency: 9.912767644726408e-6
allele num: 100880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+42G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-932G>A
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+42G>A
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

10-6264990-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264990
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264989
    reference: chr 10
allele count: 1
allele frequency: 9.987814865863646e-6
allele num: 100122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369108
  ensembl transcript: ENST00000379782
  gene symbol: PFKFB3
  hgvsc: ENST00000379782.3:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000443319
  ensembl transcript: ENST00000536985
  gene symbol: PFKFB3
  hgvsc: ENST00000536985.1:c.*414-930delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl transcript: ENST00000487989
  gene symbol: PFKFB3
  hgvsc: ENST00000487989.1:n.277+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000433771
  ensembl transcript: ENST00000461744
  gene symbol: PFKFB3
  hgvsc: ENST00000461744.1:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369115
  ensembl transcript: ENST00000379789
  gene symbol: PFKFB3
  hgvsc: ENST00000379789.4:c.1153+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000436885
  ensembl transcript: ENST00000490474
  gene symbol: PFKFB3
  hgvsc: ENST00000490474.1:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+44delA
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: GA
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

10-6264998-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6264998
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 6264998
    reference: chr 10
allele count: 1042
allele frequency: 1.171708085010683e-2
allele num: 88930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000390285
  ensembl transcript: ENST00000450232
  gene symbol: PFKFB3
  hgvsc: ENST00000450232.1:c.254+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000434628
  ensembl transcript: ENST00000467491
  gene symbol: PFKFB3
  hgvsc: ENST00000467491.1:c.1213+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000353712
  ensembl transcript: ENST00000360521
  gene symbol: PFKFB3
  hgvsc: ENST00000360521.2:c.1213+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369111
  ensembl transcript: ENST00000379785
  gene symbol: PFKFB3
  hgvsc: ENST00000379785.1:c.1213+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369105
  ensembl transcript: ENST00000317350
  gene symbol: PFKFB3
  hgvsc: ENST00000317350.4:c.1213+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000369100
  ensembl transcript: ENST00000379775
  gene symbol: PFKFB3
  hgvsc: ENST00000379775.4:c.1213+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000432356
  ensembl transcript: ENST00000477914
  gene symbol: PFKFB3
  hgvsc: ENST00000477914.1:c.1213+51C>T
  variant of: http://identifiers.org/hgnc/8874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170525
  ensembl protein: ENSP00000446384
  ensembl transcript: ENST00000540253
  gene symbol: PFKFB3
  hgvsc: ENST00000540253.1:c.1255+51C>T
  variant of: http://identifiers.org/hgnc/8874
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 20
reference allele: C

GenotypeDepth
all individuals: 12665
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9098
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 466
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.238839385662473e-5
allele num: 44666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11840
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.359e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.194e0

DP
type: SiteQuality
SIO_000300: 9.42316e5

VQSLOD
type: SiteQuality
SIO_000300: 3.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 9.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

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

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.370229912301493e-5
allele num: 42190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.38e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 8.86644e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 7.72e0

GenotypeDepth
all individuals: 8108
bin: 2.75e1
variant carriers: 1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1608
bin: 3.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
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variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3819
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17073
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6760
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.742933029785619e-5
allele num: 42168
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.442e0

DP
type: SiteQuality
SIO_000300: 8.86046e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 1.444e1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

GenotypeDepth
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
all individuals: 348
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variant carriers: 0

GenotypeQuality
all individuals: 4884
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variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29809
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1892
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.509662199467951e-5
allele num: 39846
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.41612e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.524e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

GenotypeDepth
all individuals: 1
bin: 6.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1
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variant carriers: 1

GenotypeDepth
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 1

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7389
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 287
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 1

GenotypeQuality
all individuals: 10639
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2062
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.676393565282454e-4
allele num: 10692
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3710
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 1.1062e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

QD
type: SiteQuality
SIO_000300: 1.164e1

DP
type: SiteQuality
SIO_000300: 7.62904e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeDepth
all individuals: 2301
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
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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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variant carriers: 0

GenotypeDepth
all individuals: 5
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GenotypeQuality
all individuals: 795
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GenotypeQuality
all individuals: 100
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GenotypeQuality
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GenotypeQuality
all individuals: 7992
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GenotypeQuality
all individuals: 2010
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1526
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 9796
bin: 6.25e1
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GenotypeQuality
all individuals: 268
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GenotypeQuality
all individuals: 454
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 266
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GenotypeQuality
all individuals: 253
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
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variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4778
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.82326369282891e-4
allele num: 3542
num of homozygotes: 0

South 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: 418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34836
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

DP
type: SiteQuality
SIO_000300: 7.46788e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.116e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.846e0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

GenotypeDepth
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 34040
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European (Finnish)
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South Asian
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East Asian
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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FS
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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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European (Non-Finnish)
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allele frequency: 5.217845030002609e-4
allele num: 30664
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Latino
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African
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Other
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European (Finnish)
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East Asian
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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South Asian
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Other
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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Other
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MQRankSum
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QD
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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East Asian
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South Asian
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European (Non-Finnish)
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DP
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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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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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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QD
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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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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Latino
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Other
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ClippingRankSum
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MQRankSum
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DP
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 4.424778761061947e-4
allele num: 18080
num of homozygotes: 0

East Asian
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South Asian
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Other
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Latino
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African
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European (Finnish)
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BaseQRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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Other
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South Asian
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European (Non-Finnish)
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allele num: 17984
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European (Finnish)
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East Asian
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African
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

African
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allele frequency: 1.135589370883489e-4
allele num: 8806
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 58868
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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MQ
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FS
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ClippingRankSum
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VQSLOD
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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: 8788
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.695202576707916e-4
allele num: 11798
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

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

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 frequency: 0.0e0
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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SIO_000300: -9.0e-4

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 3.7e-1

DP
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SIO_000300: 1.092779e6

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8788
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5152
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.872659176029963e-4
allele num: 10680
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.080440304826418e-5
allele num: 59050
num of homozygotes: 0

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

Other
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South Asian
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FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.097603e6

QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 2.12e-1

ClippingRankSum
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ReadPosRankSum
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SIO_000300: 2.12e-1

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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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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African
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European (Non-Finnish)
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Latino
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Other
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East Asian
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8208
num of homozygotes: 0

Latino
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European (Finnish)
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African
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South Asian
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Other
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European (Non-Finnish)
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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FS
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 1.123343068973264e-4
allele num: 8902
num of homozygotes: 0

South Asian
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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Other
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QD
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BaseQRankSum
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MQRankSum
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SIO_000300: -3.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e0

ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 1.167606e6

VQSLOD
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SIO_000300: 6.35e-1

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

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: 738
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.240143369175627e-4
allele num: 8928
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60050
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 count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

ClippingRankSum
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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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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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: 24

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

South Asian
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allele frequency: 0.0e0
allele num: 12486
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: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
num of homozygotes: 0

African
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allele count: 24
allele frequency: 2.682763246143528e-3
allele num: 8946
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60170
num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.468e0

ClippingRankSum
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SIO_000300: 1.0e-1

MQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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QD
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.0e-3

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: 3

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 1.111605157847932e-4
allele num: 8996
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60362
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: 2
allele frequency: 2.414875633904854e-4
allele num: 8282
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
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DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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SIO_000300: 7.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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ClippingRankSum
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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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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: 9080
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 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: 61020
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Other
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South Asian
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East Asian
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ClippingRankSum
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FS
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VQSLOD
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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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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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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East Asian
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Other
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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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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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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Latino
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African
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East Asian
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VQSLOD
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DP
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QD
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MQRankSum
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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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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East Asian
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European (Non-Finnish)
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allele num: 62744
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Latino
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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FS
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64018
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Latino
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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East Asian
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
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MQRankSum
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FS
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QD
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BaseQRankSum
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DP
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SIO_000300: 1.416215e6

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

VQSLOD
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ClippingRankSum
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SIO_000300: -6.32e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 4
allele frequency: 2.5e-4
allele num: 16000
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64912
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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ReadPosRankSum
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SIO_000300: 7.15e-1

VQSLOD
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ClippingRankSum
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DP
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FS
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MQ
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SIO_000300: 5.899e1

MQRankSum
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BaseQRankSum
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SIO_000300: -3.326e0

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

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

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

South Asian
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

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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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: 1
allele frequency: 1.54054720236628e-5
allele num: 64912
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.326e0

FS
type: SiteQuality
SIO_000300: 1.2967e1

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

DP
type: SiteQuality
SIO_000300: 1.418353e6

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

ClippingRankSum
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SIO_000300: -5.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.677e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5894
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544306143249838e-5
allele num: 64754
num of homozygotes: 0

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.106e0

FS
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SIO_000300: 3.709e0

DP
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SIO_000300: 1.415245e6

InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 5.659999999999999e-1

MQ
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SIO_000300: 5.96e1

ClippingRankSum
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SIO_000300: -2.71e-1

MQRankSum
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SIO_000300: -3.36e-1

QD
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SIO_000300: 3.349e1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 16

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

European (Non-Finnish)
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allele count: 62
allele frequency: 9.875756610385473e-4
allele num: 62780
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European (Finnish)
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allele frequency: 1.714285714285714e-3
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African
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allele count: 30
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East Asian
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ClippingRankSum
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FS
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MQRankSum
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QD
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 385

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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South Asian
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allele count: 64
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allele num: 16034
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European (Non-Finnish)
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allele frequency: 4.580908753249969e-3
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East Asian
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African
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Latino
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Other
type: Population
allele count: 8
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allele num: 846
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European (Finnish)
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allele count: 2
allele frequency: 3.424657534246575e-4
allele num: 5840
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FS
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 2.357378595002357e-4
allele num: 8484
num of homozygotes: 0

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

Other
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num of homozygotes: 0

MQ
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MQRankSum
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VQSLOD
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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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

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

European (Finnish)
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allele frequency: 0.0e0
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African
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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

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

Latino
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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DP
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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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

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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.55724430048586e-5
allele num: 64216
num of homozygotes: 0

Other
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num of homozygotes: 0

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

East Asian
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allele num: 8460
num of homozygotes: 0

Other
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

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

Latino
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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QD
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ReadPosRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 2.763957987838585e-4
allele num: 10854
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63310
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

MQ
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SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.358585e6

QD
type: SiteQuality
SIO_000300: 1.238e1

FS
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SIO_000300: 2.054e0

VQSLOD
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BaseQRankSum
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SIO_000300: 1.07e0

MQRankSum
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SIO_000300: -1.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-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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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: 8356
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.889644746787604e-4
allele num: 5292
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.586193769430874e-5
allele num: 63044
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

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQ
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SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 4.765e0

DP
type: SiteQuality
SIO_000300: 1.343405e6

ClippingRankSum
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VQSLOD
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SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

InbreedingCoeff
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SIO_000300: 5.0e-4

BaseQRankSum
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SIO_000300: -1.416e0

QD
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SIO_000300: 1.421e1

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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variant carriers: 5

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 8.120046771469404e-5
allele num: 61576
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10538
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.263094e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

FS
type: SiteQuality
SIO_000300: 1.993e1

BaseQRankSum
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SIO_000300: 6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.597e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

GenotypeDepth
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variant carriers: 12

GenotypeDepth
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variant carriers: 21

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5032
num of homozygotes: 0

African
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allele count: 249
allele frequency: 2.744104033502314e-2
allele num: 9074
num of homozygotes: 2

South Asian
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allele count: 1
allele frequency: 6.791632708503124e-5
allele num: 14724
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
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Latino
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allele count: 12
allele frequency: 1.138736003036629e-3
allele num: 10538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.123740820172873e-5
allele num: 61548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
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SIO_000300: 1.467e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.87e-1

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

DP
type: SiteQuality
SIO_000300: 1.263861e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-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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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: 8200
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5032
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14724
num of homozygotes: 0

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

Other
type: Population
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.624748164034575e-5
allele num: 61548
num of homozygotes: 0

QD
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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MQ
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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African
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Latino
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South Asian
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Other
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European (Finnish)
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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FS
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BaseQRankSum
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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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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

European (Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 4888
num of homozygotes: 0

Other
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.941362498352879e-5
allele num: 60712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8906
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 1.190557e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.113e1

GenotypeDepth
all individuals: 5841
bin: 7.5e0
variant carriers: 25

GenotypeDepth
all individuals: 4336
bin: 1.75e1
variant carriers: 107

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 163
bin: 4.75e1
variant carriers: 7

GenotypeDepth
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1101
bin: 9.75e1
variant carriers: 607

GenotypeQuality
all individuals: 16055
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 185
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2991
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3482
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 876
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 26989
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 283
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 91
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 540
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 555
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 642
bin: 5.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 78
allele frequency: 1.612903225806452e-2
allele num: 4836
num of homozygotes: 1

Other
type: Population
allele count: 5
allele frequency: 6.544502617801047e-3
allele num: 764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 453
allele frequency: 7.486118455843469e-3
allele num: 60512
num of homozygotes: 1

Latino
type: Population
allele count: 26
allele frequency: 2.505782575173477e-3
allele num: 10376
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.015113918339725e-3
allele num: 8866
num of homozygotes: 0

South Asian
type: Population
allele count: 50
allele frequency: 3.490645071209159e-3
allele num: 14324
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

QD
type: SiteQuality
SIO_000300: 1.297e1

FS
type: SiteQuality
SIO_000300: 5.77e-1

DP
type: SiteQuality
SIO_000300: 1.168396e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11569
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variant carriers: 4

GenotypeDepth
all individuals: 25
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variant carriers: 0

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeDepth
all individuals: 9
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variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 511
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variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
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variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3721
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variant carriers: 0

GenotypeQuality
all individuals: 26055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 602
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variant carriers: 0

GenotypeQuality
all individuals: 16823
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3709
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variant carriers: 0

GenotypeQuality
all individuals: 2856
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variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14156
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.326259946949602e-3
allele num: 754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.660633033312299e-5
allele num: 60218
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.160541586073501e-3
allele num: 10340
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

VQSLOD
type: SiteQuality
SIO_000300: 5.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 1.786e0

DP
type: SiteQuality
SIO_000300: 1.149539e6

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10822
bin: 2.75e1
variant carriers: 13

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15340
bin: 2.25e1
variant carriers: 21

GenotypeDepth
all individuals: 15
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18293
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 17884
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4317
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 333
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 84
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 238
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variant carriers: 1

GenotypeQuality
all individuals: 568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 23379
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 9.75e1
variant carriers: 60

European (Non-Finnish)
type: Population
allele count: 58
allele frequency: 9.707762862785793e-4
allele num: 59746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.91601866251944e-4
allele num: 10288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8720
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.147766323024055e-4
allele num: 4656
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.119212e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.195e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeDepth
all individuals: 63
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variant carriers: 0

GenotypeDepth
all individuals: 2170
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variant carriers: 0

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 333
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variant carriers: 0

GenotypeQuality
all individuals: 568
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GenotypeQuality
all individuals: 4218
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variant carriers: 0

GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
all individuals: 1168
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variant carriers: 0

GenotypeQuality
all individuals: 17884
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 497
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variant carriers: 0

GenotypeQuality
all individuals: 556
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variant carriers: 1

GenotypeQuality
all individuals: 4317
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 238
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variant carriers: 0

GenotypeQuality
all individuals: 2684
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variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 23379
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variant carriers: 0

GenotypeQuality
all individuals: 459
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variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.147766323024055e-4
allele num: 4656
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.195e1

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 1.119212e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

GenotypeDepth
all individuals: 10064
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 19474
bin: 1.25e1
variant carriers: 3

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeDepth
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 18686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21078
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 7.5e0
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GenotypeQuality
all individuals: 2296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4632
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variant carriers: 0

GenotypeQuality
all individuals: 457
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variant carriers: 0

GenotypeQuality
all individuals: 227
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GenotypeQuality
all individuals: 367
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GenotypeQuality
all individuals: 4863
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variant carriers: 0

GenotypeQuality
all individuals: 538
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variant carriers: 0

GenotypeQuality
all individuals: 2446
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variant carriers: 0

GenotypeQuality
all individuals: 154
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GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 447
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GenotypeQuality
all individuals: 507
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 599
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variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4628
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.155123068116771e-5
allele num: 13976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.679938178275039e-4
allele num: 59526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8692
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.671e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.097e0

DP
type: SiteQuality
SIO_000300: 1.09309e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.085e1

GenotypeDepth
all individuals: 15670
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 9
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variant carriers: 0

GenotypeDepth
all individuals: 262
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variant carriers: 0

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 8308
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GenotypeQuality
all individuals: 804
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GenotypeQuality
all individuals: 6324
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variant carriers: 0

GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 337
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GenotypeQuality
all individuals: 1087
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variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 278
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GenotypeQuality
all individuals: 2800
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GenotypeQuality
all individuals: 10203
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variant carriers: 0

GenotypeQuality
all individuals: 1243
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GenotypeQuality
all individuals: 1456
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20155
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variant carriers: 0

GenotypeQuality
all individuals: 5076
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GenotypeQuality
all individuals: 1060
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 220
bin: 5.25e1
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GenotypeQuality
all individuals: 496
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variant carriers: 1

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.742646033737627e-5
allele num: 57384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.054e1

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 9.62485e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

FS
type: SiteQuality
SIO_000300: 2.541e0

VQSLOD
type: SiteQuality
SIO_000300: -6.969e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeDepth
all individuals: 21
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variant carriers: 0

GenotypeDepth
all individuals: 33
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variant carriers: 0

GenotypeDepth
all individuals: 16381
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variant carriers: 0

GenotypeDepth
all individuals: 9
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GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 1270
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variant carriers: 0

GenotypeQuality
all individuals: 19842
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5435
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6387
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8486
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.271940981938438e-4
allele num: 7862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13168
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.341e0

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.287e0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

DP
type: SiteQuality
SIO_000300: 9.53638e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 20850
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1304
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6419
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5776
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.662835249042145e-5
allele num: 13050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 6.16e1

FS
type: SiteQuality
SIO_000300: 4.506e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.49e-1

QD
type: SiteQuality
SIO_000300: 2.093e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

DP
type: SiteQuality
SIO_000300: 9.45628e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0