1-74671077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671077
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671077
    reference: chr 1
allele count: 36
allele frequency: 2.965257071314433e-4
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+3983C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+3983C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+3983C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+3983C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+3983C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1385C>T
  hgvsp: ENSP00000359935.3:p.Ala462Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1346C>T
  hgvsp: ENSP00000476680.1:p.Ala449Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.584C>T
  hgvsp: ENSP00000432819.1:p.Ala195Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+937C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+3983C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*19C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+3983C>T
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala449Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

1-74671079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671079
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671079
    reference: chr 1
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+3985C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1348C>T
  hgvsp: ENSP00000476680.1:p.His450Tyr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.586C>T
  hgvsp: ENSP00000432819.1:p.His196Tyr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*21C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+3985C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1387C>T
  hgvsp: ENSP00000359935.3:p.His463Tyr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+3985C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+3985C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+3985C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+3985C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+3985C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+939C>T
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His450Tyr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

1-74671080-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671080
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671079
    reference: chr 1
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.589delT
  hgvsp: ENSP00000432819.1:p.Ser197LeufsTer6
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+3988delT
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*24delT
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1390delT
  hgvsp: ENSP00000359935.3:p.Ser464LeufsTer6
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1351delT
  hgvsp: ENSP00000476680.1:p.Ser451LeufsTer6
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+3988delT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+3988delT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+3988delT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+942delT
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+3988delT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+3988delT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+3988delT
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser451LeufsTer6
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: AT
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

1-74671088-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671088
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671088
    reference: chr 1
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+3994G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+3994G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*30G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+948G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1396G>C
  hgvsp: ENSP00000359935.3:p.Val466Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.595G>C
  hgvsp: ENSP00000432819.1:p.Val199Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+3994G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+3994G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1357G>C
  hgvsp: ENSP00000476680.1:p.Val453Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+3994G>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+3994G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+3994G>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val453Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

1-74671117-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671117
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671117
    reference: chr 1
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.624A>G
  hgvsp: ENST00000534056.1:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+977A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4023A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4023A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1425A>G
  hgvsp: ENST00000370898.3:c.1425A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4023A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4023A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1386A>G
  hgvsp: ENST00000609362.1:c.1386A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*59A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4023A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4023A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4023A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg462Arg
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

1-74671127-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671127
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671127
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4033T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4033T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1435T>C
  hgvsp: ENSP00000359935.3:p.Tyr479His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.634T>C
  hgvsp: ENSP00000432819.1:p.Tyr212His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4033T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*69T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4033T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4033T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4033T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1396T>C
  hgvsp: ENSP00000476680.1:p.Tyr466His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+987T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4033T>C
  variant of: http://identifiers.org/hgnc/19661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr466His
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-74671132-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671132
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671132
    reference: chr 1
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1401A>G
  hgvsp: ENST00000609362.1:c.1401A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4038A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.639A>G
  hgvsp: ENST00000534056.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4038A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1440A>G
  hgvsp: ENST00000370898.3:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*74A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4038A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4038A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4038A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4038A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4038A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+992A>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala467Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

1-74671135-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671135
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671135
    reference: chr 1
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4041T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4041T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4041T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1404T>G
  hgvsp: ENST00000609362.1:c.1404T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4041T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*77T>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1443T>G
  hgvsp: ENST00000370898.3:c.1443T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4041T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.642T>G
  hgvsp: ENST00000534056.1:c.642T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4041T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4041T>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+995T>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr468Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

1-74671136-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671136
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671136
    reference: chr 1
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4042A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4042A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4042A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.643A>G
  hgvsp: ENSP00000432819.1:p.Met215Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1444A>G
  hgvsp: ENSP00000359935.3:p.Met482Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4042A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*78A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4042A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4042A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1405A>G
  hgvsp: ENSP00000476680.1:p.Met469Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4042A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+996A>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met469Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/1-74671158-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671158
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671158
    reference: chr 1
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4064A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1466A>C
  hgvsp: ENSP00000359935.3:p.Asn489Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1018A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4064A>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1427A>C
  hgvsp: ENSP00000476680.1:p.Asn476Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4064A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4064A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.665A>C
  hgvsp: ENSP00000432819.1:p.Asn222Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4064A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4064A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*100A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4064A>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn476Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-74671167-A-ATTTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671167
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671171
    reference: chr 1
allele count: 18
allele frequency: 1.483019427554501e-4
allele num: 121374
alternate allele: ATTTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4073_343+4074insTTTC
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1436_1437insTTTC
  hgvsp: ENSP00000476680.1:p.Lys479AsnfsTer30
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.674_675insTTTC
  hgvsp: ENSP00000432819.1:p.Lys225AsnfsTer30
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4073_343+4074insTTTC
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4073_369+4074insTTTC
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1475_1476insTTTC
  hgvsp: ENSP00000359935.3:p.Lys492AsnfsTer30
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4073_382+4074insTTTC
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4073_343+4074insTTTC
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4073_343+4074insTTTC
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1027_448+1028insTTTC
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4073_343+4074insTTTC
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*109_*110insTTTC
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys479AsnfsTer30
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

1-74671170-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671170
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671170
    reference: chr 1
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1478G>A
  hgvsp: ENSP00000359935.3:p.Ser493Asn
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4076G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*112G>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4076G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4076G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4076G>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.677G>A
  hgvsp: ENSP00000432819.1:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1439G>A
  hgvsp: ENSP00000476680.1:p.Ser480Asn
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4076G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4076G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4076G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1030G>A
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser480Asn
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

1-74671176-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671176
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671176
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4082A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4082A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*118A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1484A>G
  hgvsp: ENSP00000359935.3:p.Lys495Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4082A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.683A>G
  hgvsp: ENSP00000432819.1:p.Lys228Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4082A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1445A>G
  hgvsp: ENSP00000476680.1:p.Lys482Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4082A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4082A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1036A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4082A>G
  variant of: http://identifiers.org/hgnc/19661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys482Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

1-74671180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671180
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671180
    reference: chr 1
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.687A>G
  hgvsp: ENST00000534056.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1449A>G
  hgvsp: ENST00000609362.1:c.1449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4086A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*122A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4086A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1488A>G
  hgvsp: ENST00000370898.3:c.1488A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4086A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1040A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4086A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4086A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4086A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4086A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr483Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

1-74671185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671185
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671185
    reference: chr 1
allele count: 8
allele frequency: 6.591197455797781e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1454C>T
  hgvsp: ENSP00000476680.1:p.Ser485Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1045C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4091C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4091C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4091C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4091C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4091C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.692C>T
  hgvsp: ENSP00000432819.1:p.Ser231Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4091C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*127C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1493C>T
  hgvsp: ENSP00000359935.3:p.Ser498Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4091C>T
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser485Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-74671190-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671190
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671190
    reference: chr 1
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1050A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1498A>G
  hgvsp: ENSP00000359935.3:p.Ile500Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4096A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4096A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4096A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4096A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4096A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1459A>G
  hgvsp: ENSP00000476680.1:p.Ile487Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4096A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4096A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*132A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.697A>G
  hgvsp: ENSP00000432819.1:p.Ile233Val
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile487Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

1-74671197-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671197
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671197
    reference: chr 1
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4103T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4103T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4103T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4103T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4103T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.704T>C
  hgvsp: ENSP00000432819.1:p.Leu235Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*139T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4103T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1466T>C
  hgvsp: ENSP00000476680.1:p.Leu489Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1505T>C
  hgvsp: ENSP00000359935.3:p.Leu502Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1057T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4103T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu489Ser
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

1-74671199-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671199
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671199
    reference: chr 1
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4105C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1059C>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.706C>G
  hgvsp: ENSP00000432819.1:p.Leu236Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4105C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*141C>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1507C>G
  hgvsp: ENSP00000359935.3:p.Leu503Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1468C>G
  hgvsp: ENSP00000476680.1:p.Leu490Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4105C>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4105C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4105C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4105C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4105C>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu490Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-74671204-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671204
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671204
    reference: chr 1
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4110A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1512A>G
  hgvsp: ENST00000370898.3:c.1512A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*146A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4110A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4110A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.711A>G
  hgvsp: ENST00000534056.1:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4110A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4110A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1473A>G
  hgvsp: ENST00000609362.1:c.1473A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1064A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4110A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4110A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln491Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-74671207-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671207
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671207
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4113C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*149C>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4113C>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4113C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4113C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4113C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1476C>A
  hgvsp: ENSP00000476680.1:p.Phe492Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4113C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4113C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.714C>A
  hgvsp: ENSP00000432819.1:p.Phe238Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1515C>A
  hgvsp: ENSP00000359935.3:p.Phe505Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1067C>A
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe492Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-74671207-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671207
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671207
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4113C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*149C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4113C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1067C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1515C>T
  hgvsp: ENST00000370898.3:c.1515C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.714C>T
  hgvsp: ENST00000534056.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4113C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4113C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4113C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1476C>T
  hgvsp: ENST00000609362.1:c.1476C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4113C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4113C>T
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe492Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

1-74671210-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671210
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671209
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4118delG
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4118delG
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4118delG
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1520delG
  hgvsp: ENSP00000359935.3:p.Gly507GlufsTer8
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4118delG
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4118delG
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1481delG
  hgvsp: ENSP00000476680.1:p.Gly494GlufsTer8
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.719delG
  hgvsp: ENSP00000432819.1:p.Gly240GlufsTer8
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4118delG
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1072delG
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*154delG
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4118delG
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20707
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly494GlufsTer8
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: TG
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

1-74671211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671211
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671211
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4117G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4117G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1480G>A
  hgvsp: ENSP00000476680.1:p.Gly494Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4117G>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1519G>A
  hgvsp: ENSP00000359935.3:p.Gly507Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4117G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4117G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.718G>A
  hgvsp: ENSP00000432819.1:p.Gly240Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1071G>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4117G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*153G>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4117G>A
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20705
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly494Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

1-74671212-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671212
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671212
    reference: chr 1
allele count: 7
allele frequency: 5.76710771309463e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.719G>T
  hgvsp: ENSP00000432819.1:p.Gly240Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4118G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4118G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4118G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4118G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*154G>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1481G>T
  hgvsp: ENSP00000476680.1:p.Gly494Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1072G>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4118G>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4118G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1520G>T
  hgvsp: ENSP00000359935.3:p.Gly507Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4118G>T
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly494Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-74671213-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671213
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671213
    reference: chr 1
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1073A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4119A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4119A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4119A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1521A>C
  hgvsp: ENST00000370898.3:c.1521A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*155A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4119A>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1482A>C
  hgvsp: ENST00000609362.1:c.1482A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4119A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4119A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4119A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.720A>C
  hgvsp: ENST00000534056.1:c.720A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly494Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

1-74671220-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671220
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671220
    reference: chr 1
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4126T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*162T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4126T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4126T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4126T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4126T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1528T>C
  hgvsp: ENSP00000359935.3:p.Phe510Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4126T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.727T>C
  hgvsp: ENSP00000432819.1:p.Phe243Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1489T>C
  hgvsp: ENSP00000476680.1:p.Phe497Leu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1080T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4126T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe497Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

1-74671225-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671225
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671225
    reference: chr 1
allele count: 4
allele frequency: 3.295435821387378e-5
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4131G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*167G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4131G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4131G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.732G>C
  hgvsp: ENST00000534056.1:c.732G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4131G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4131G>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1494G>C
  hgvsp: ENST00000609362.1:c.1494G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1533G>C
  hgvsp: ENST00000370898.3:c.1533G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4131G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1085G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4131G>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu498Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

1-74671232-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671232
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671232
    reference: chr 1
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1501T>G
  hgvsp: ENSP00000476680.1:p.Leu501Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4138T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4138T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*174T>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1540T>G
  hgvsp: ENSP00000359935.3:p.Leu514Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4138T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1092T>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4138T>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4138T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4138T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.739T>G
  hgvsp: ENSP00000432819.1:p.Leu247Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4138T>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu501Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-74671249-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671249
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671248
    reference: chr 1
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4158delA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1560delA
  hgvsp: ENSP00000359935.3:p.Val521LeufsTer13
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.759delA
  hgvsp: ENSP00000432819.1:p.Val254LeufsTer13
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4158delA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1521delA
  hgvsp: ENSP00000476680.1:p.Val508LeufsTer13
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1112delA
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4158delA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*194delA
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4158delA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4158delA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4158delA
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4158delA
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val508LeufsTer13
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: TA
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

1-74671264-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671264
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671264
    reference: chr 1
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4170A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4170A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4170A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.771A>G
  hgvsp: ENST00000534056.1:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4170A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1533A>G
  hgvsp: ENST00000609362.1:c.1533A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4170A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4170A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1572A>G
  hgvsp: ENST00000370898.3:c.1572A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*206A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1124A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4170A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu511Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

1-74671275-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671275
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671275
    reference: chr 1
allele count: 16
allele frequency: 1.318239491159556e-4
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4181G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1544G>T
  hgvsp: ENSP00000476680.1:p.Gly515Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.782G>T
  hgvsp: ENSP00000432819.1:p.Gly261Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1135G>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4181G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4181G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4181G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4181G>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1583G>T
  hgvsp: ENSP00000359935.3:p.Gly528Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4181G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4181G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*217G>T
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly515Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

1-74671278-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671278
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671278
    reference: chr 1
allele count: 4
allele frequency: 3.295598727898891e-5
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4184A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4184A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4184A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4184A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1586A>G
  hgvsp: ENSP00000359935.3:p.Asn529Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4184A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1547A>G
  hgvsp: ENSP00000476680.1:p.Asn516Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.785A>G
  hgvsp: ENSP00000432819.1:p.Asn262Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4184A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*220A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4184A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1138A>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Asn516Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/1-74671281-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671281
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671281
    reference: chr 1
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.788A>C
  hgvsp: ENSP00000432819.1:p.Lys263Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*223A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4187A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4187A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1550A>C
  hgvsp: ENSP00000476680.1:p.Lys517Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4187A>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4187A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1141A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4187A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4187A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4187A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1589A>C
  hgvsp: ENSP00000359935.3:p.Lys530Thr
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys517Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

1-74671283-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671283
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671283
    reference: chr 1
allele count: 294
allele frequency: 2.422225151595043e-3
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*225A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4189A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1591A>G
  hgvsp: ENSP00000359935.3:p.Thr531Ala
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4189A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4189A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4189A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1552A>G
  hgvsp: ENSP00000476680.1:p.Thr518Ala
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.790A>G
  hgvsp: ENSP00000432819.1:p.Thr264Ala
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4189A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4189A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1143A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4189A>G
  variant of: http://identifiers.org/hgnc/19661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20706
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
hgvs: p.Thr518Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

1-74671306-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671306
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671306
    reference: chr 1
allele count: 4
allele frequency: 3.296033224014898e-5
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4212A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*248A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.813A>G
  hgvsp: ENST00000534056.1:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1575A>G
  hgvsp: ENST00000609362.1:c.1575A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1166A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4212A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4212A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4212A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4212A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4212A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1614A>G
  hgvsp: ENST00000370898.3:c.1614A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4212A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala525Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/1-74671307-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671307
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671307
    reference: chr 1
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1615C>A
  hgvsp: ENSP00000359935.3:p.Arg539Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1576C>A
  hgvsp: ENSP00000476680.1:p.Arg526Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1167C>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*249C>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4213C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4213C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4213C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.814C>A
  hgvsp: ENSP00000432819.1:p.Arg272Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4213C>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4213C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4213C>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4213C>A
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg526Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

1-74671307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671307
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671307
    reference: chr 1
allele count: 4
allele frequency: 3.296087544085171e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*249C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1615C>T
  hgvsp: ENSP00000359935.3:p.Arg539Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.814C>T
  hgvsp: ENSP00000432819.1:p.Arg272Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4213C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4213C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1576C>T
  hgvsp: ENSP00000476680.1:p.Arg526Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4213C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4213C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4213C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1167C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4213C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4213C>T
  variant of: http://identifiers.org/hgnc/19661
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg526Cys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-74671308-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671308
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671308
    reference: chr 1
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4214G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1616G>A
  hgvsp: ENSP00000359935.3:p.Arg539His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1577G>A
  hgvsp: ENSP00000476680.1:p.Arg526His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4214G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.815G>A
  hgvsp: ENSP00000432819.1:p.Arg272His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*250G>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4214G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1168G>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4214G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4214G>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4214G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4214G>A
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20760
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg526His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

1-74671309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671309
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671309
    reference: chr 1
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4215C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4215C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4215C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1617C>T
  hgvsp: ENST00000370898.3:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.816C>T
  hgvsp: ENST00000534056.1:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4215C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4215C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1578C>T
  hgvsp: ENST00000609362.1:c.1578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4215C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4215C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*251C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1169C>T
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg526Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

1-74671311-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671311
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671311
    reference: chr 1
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4217T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4217T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1580T>G
  hgvsp: ENSP00000476680.1:p.Ile527Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1171T>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4217T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4217T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1619T>G
  hgvsp: ENSP00000359935.3:p.Ile540Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*253T>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.818T>G
  hgvsp: ENSP00000432819.1:p.Ile273Ser
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4217T>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4217T>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4217T>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile527Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

1-74671323-GTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671323
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671320
    reference: chr 1
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4235_343+4237delCTT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1637_1639delCTT
  hgvsp: ENSP00000359935.3:p.Ser546del
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4235_343+4237delCTT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1189_448+1191delCTT
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*271_*273delCTT
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4235_369+4237delCTT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.836_838delCTT
  hgvsp: ENSP00000432819.1:p.Ser279del
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4235_382+4237delCTT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4235_343+4237delCTT
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1598_1600delCTT
  hgvsp: ENSP00000476680.1:p.Ser533del
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4235_343+4237delCTT
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4235_343+4237delCTT
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser533del
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: GTTC
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

1-74671326-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671326
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671326
    reference: chr 1
allele count: 3
allele frequency: 2.472432378974435e-5
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4232C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4232C>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.833C>G
  hgvsp: ENSP00000432819.1:p.Ser278Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*268C>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4232C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1634C>G
  hgvsp: ENSP00000359935.3:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1595C>G
  hgvsp: ENSP00000476680.1:p.Ser532Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4232C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4232C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4232C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4232C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1186C>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser532Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-74671331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671331
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671331
    reference: chr 1
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1191T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4237T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4237T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4237T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1600T>C
  hgvsp: ENST00000609362.1:c.1600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*273T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4237T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4237T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.838T>C
  hgvsp: ENST00000534056.1:c.838T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1639T>C
  hgvsp: ENST00000370898.3:c.1639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4237T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4237T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu534Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

1-74671331-TTGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671331
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671327
    reference: chr 1
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4241_343+4244delGTGA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1604_1607delGTGA
  hgvsp: ENSP00000476680.1:p.Ser535ThrfsTer4
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4241_343+4244delGTGA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.842_845delGTGA
  hgvsp: ENSP00000432819.1:p.Ser281ThrfsTer4
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1643_1646delGTGA
  hgvsp: ENSP00000359935.3:p.Ser548ThrfsTer4
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4241_369+4244delGTGA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4241_382+4244delGTGA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4241_343+4244delGTGA
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*277_*280delGTGA
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1195_448+1198delGTGA
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4241_343+4244delGTGA
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4241_343+4244delGTGA
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser535ThrfsTer4
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: TTGAG
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

1-74671333-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671333
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671333
    reference: chr 1
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4239G>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4239G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4239G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4239G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4239G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1641G>C
  hgvsp: ENSP00000359935.3:p.Leu547Phe
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1602G>C
  hgvsp: ENSP00000476680.1:p.Leu534Phe
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1193G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.840G>C
  hgvsp: ENSP00000432819.1:p.Leu280Phe
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*275G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4239G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4239G>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu534Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-74671334-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671334
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671334
    reference: chr 1
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1194A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.841A>G
  hgvsp: ENSP00000432819.1:p.Ser281Gly
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*276A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4240A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4240A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1603A>G
  hgvsp: ENSP00000476680.1:p.Ser535Gly
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1642A>G
  hgvsp: ENSP00000359935.3:p.Ser548Gly
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4240A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4240A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4240A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4240A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4240A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser535Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-74671335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671335
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671335
    reference: chr 1
allele count: 4
allele frequency: 3.29663084327817e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4241G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1643G>A
  hgvsp: ENSP00000359935.3:p.Ser548Asn
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4241G>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1604G>A
  hgvsp: ENSP00000476680.1:p.Ser535Asn
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*277G>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4241G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4241G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4241G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4241G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.842G>A
  hgvsp: ENSP00000432819.1:p.Ser281Asn
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4241G>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1195G>A
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser535Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

1-74671342-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671342
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671342
    reference: chr 1
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*284A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1611A>G
  hgvsp: ENST00000609362.1:c.1611A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.849A>G
  hgvsp: ENST00000534056.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4248A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4248A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4248A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4248A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4248A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1650A>G
  hgvsp: ENST00000370898.3:c.1650A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4248A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1202A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4248A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser537Ser
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-74671344-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671344
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671344
    reference: chr 1
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4250T>A
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1204T>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.851T>A
  hgvsp: ENSP00000432819.1:p.Val284Asp
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4250T>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4250T>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4250T>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1613T>A
  hgvsp: ENSP00000476680.1:p.Val538Asp
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1652T>A
  hgvsp: ENSP00000359935.3:p.Val551Asp
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4250T>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*286T>A
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4250T>A
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4250T>A
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val538Asp
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD

1-74671345-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671345
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671345
    reference: chr 1
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*287T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.852T>C
  hgvsp: ENST00000534056.1:c.852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1205T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4251T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4251T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1653T>C
  hgvsp: ENST00000370898.3:c.1653T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4251T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1614T>C
  hgvsp: ENST00000609362.1:c.1614T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4251T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4251T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4251T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4251T>C
  variant of: http://identifiers.org/hgnc/19661
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val538Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-74671354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671354
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671354
    reference: chr 1
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4260C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4260C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4260C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4260C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4260C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.861C>T
  hgvsp: ENST00000534056.1:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4260C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4260C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1623C>T
  hgvsp: ENST00000609362.1:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1662C>T
  hgvsp: ENST00000370898.3:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*296C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1214C>T
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser541Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

1-74671358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671358
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671358
    reference: chr 1
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4264A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.865A>G
  hgvsp: ENSP00000432819.1:p.Lys289Glu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4264A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1666A>G
  hgvsp: ENSP00000359935.3:p.Lys556Glu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4264A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4264A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*300A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1627A>G
  hgvsp: ENSP00000476680.1:p.Lys543Glu
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1218A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4264A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4264A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4264A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys543Glu
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-74671361-ATGTTAAATGC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671361
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671351
    reference: chr 1
allele count: 5
allele frequency: 4.121875618281343e-5
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsp: ENSP00000476680.1:p.Asn546ArgfsTer8
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsp: ENSP00000432819.1:p.Asn292ArgfsTer8
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsp: ENSP00000359935.3:p.Asn559ArgfsTer8
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7912
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn546ArgfsTer8
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: ATGTTAAATGC
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

1-74671366-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671366
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671366
    reference: chr 1
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4272A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4272A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4272A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4272A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4272A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4272A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1226A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1635A>G
  hgvsp: ENST00000609362.1:c.1635A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.873A>G
  hgvsp: ENST00000534056.1:c.873A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1674A>G
  hgvsp: ENST00000370898.3:c.1674A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4272A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*308A>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu545Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

1-74671372-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671372
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671372
    reference: chr 1
allele count: 3
allele frequency: 2.473696362017217e-5
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4278T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4278T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.879T>C
  hgvsp: ENST00000534056.1:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*314T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1680T>C
  hgvsp: ENST00000370898.3:c.1680T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1641T>C
  hgvsp: ENST00000609362.1:c.1641T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4278T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4278T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1232T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4278T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4278T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4278T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala547Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-74671377-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671377
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671377
    reference: chr 1
allele count: 59
allele frequency: 4.86493617863386e-4
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*319A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1685A>C
  hgvsp: ENSP00000359935.3:p.Lys562Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4283A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4283A>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4283A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4283A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1237A>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1646A>C
  hgvsp: ENSP00000476680.1:p.Lys549Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.884A>C
  hgvsp: ENSP00000432819.1:p.Lys295Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4283A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4283A>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4283A>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Lys549Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-74671383-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671383
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671383
    reference: chr 1
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1243A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4289A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4289A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4289A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4289A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1691A>G
  hgvsp: ENSP00000359935.3:p.Lys564Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.890A>G
  hgvsp: ENSP00000432819.1:p.Lys297Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1652A>G
  hgvsp: ENSP00000476680.1:p.Lys551Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4289A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4289A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4289A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*325A>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys551Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-74671395-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671395
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671395
    reference: chr 1
allele count: 2
allele frequency: 1.649892756970797e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4301G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4301G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4301G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1255G>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4301G>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4301G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1703G>T
  hgvsp: ENSP00000359935.3:p.Ser568Ile
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1664G>T
  hgvsp: ENSP00000476680.1:p.Ser555Ile
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*337G>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.902G>T
  hgvsp: ENSP00000432819.1:p.Ser301Ile
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4301G>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4301G>T
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser555Ile
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-74671396-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671396
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671396
    reference: chr 1
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4302C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4302C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4302C>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4302C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1665C>G
  hgvsp: ENSP00000476680.1:p.Ser555Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4302C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4302C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1704C>G
  hgvsp: ENSP00000359935.3:p.Ser568Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4302C>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1256C>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.903C>G
  hgvsp: ENSP00000432819.1:p.Ser301Arg
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*338C>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser555Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-74671406-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671406
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671406
    reference: chr 1
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4312T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1266T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4312T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4312T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1675T>C
  hgvsp: ENSP00000476680.1:p.Tyr559His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4312T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.913T>C
  hgvsp: ENSP00000432819.1:p.Tyr305His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1714T>C
  hgvsp: ENSP00000359935.3:p.Tyr572His
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*348T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4312T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4312T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4312T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr559His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

1-74671407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671407
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671407
    reference: chr 1
allele count: 5
allele frequency: 4.127592127856294e-5
allele num: 121136
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4313A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4313A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4313A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.914A>G
  hgvsp: ENSP00000432819.1:p.Tyr305Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1676A>G
  hgvsp: ENSP00000476680.1:p.Tyr559Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4313A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*349A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1715A>G
  hgvsp: ENSP00000359935.3:p.Tyr572Cys
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1267A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4313A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4313A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4313A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10667
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr559Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

1-74671414-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671414
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671414
    reference: chr 1
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1722G>C
  hgvsp: ENSP00000359935.3:p.Leu574Phe
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1683G>C
  hgvsp: ENSP00000476680.1:p.Leu561Phe
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4320G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.921G>C
  hgvsp: ENSP00000432819.1:p.Leu307Phe
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4320G>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4320G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4320G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4320G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4320G>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*356G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1274G>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4320G>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu561Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-74671415-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671415
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671415
    reference: chr 1
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1275C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4321C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4321C>T
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4321C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4321C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4321C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1723C>T
  hgvsp: ENST00000370898.3:c.1723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1684C>T
  hgvsp: ENST00000609362.1:c.1684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*357C>T
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.922C>T
  hgvsp: ENST00000534056.1:c.922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4321C>T
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4321C>T
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20632
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu562Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

1-74671421-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671421
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671421
    reference: chr 1
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1690A>G
  hgvsp: ENSP00000476680.1:p.Ile564Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4327A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4327A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4327A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4327A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*363A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.928A>G
  hgvsp: ENSP00000432819.1:p.Ile310Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4327A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1729A>G
  hgvsp: ENSP00000359935.3:p.Ile577Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4327A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4327A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1281A>G
  variant of: http://identifiers.org/hgnc/3825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile564Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-74671431-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671431
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671431
    reference: chr 1
allele count: 1
allele frequency: 8.279379377721846e-6
allele num: 120782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4337T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1700T>C
  hgvsp: ENSP00000476680.1:p.Met567Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1291T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4337T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4337T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4337T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4337T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4337T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.938T>C
  hgvsp: ENSP00000432819.1:p.Met313Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1739T>C
  hgvsp: ENSP00000359935.3:p.Met580Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*373T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4337T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met567Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

1-74671457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671457
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671457
    reference: chr 1
allele count: 1
allele frequency: 8.361064196250898e-6
allele num: 119602
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4363A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*399A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4363A>G
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1765A>G
  hgvsp: ENSP00000359935.3:p.Met589Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1726A>G
  hgvsp: ENSP00000476680.1:p.Met576Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4363A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.964A>G
  hgvsp: ENSP00000432819.1:p.Met322Val
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4363A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4363A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1317A>G
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4363A>G
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4363A>G
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met576Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

1-74671458-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74671458
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 74671458
    reference: chr 1
allele count: 1
allele frequency: 8.361623492817366e-6
allele num: 119594
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000476680
  ensembl transcript: ENST00000609362
  gene symbol: FPGT
  hgvsc: ENST00000609362.1:c.1727T>C
  hgvsp: ENSP00000476680.1:p.Met576Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000432819
  ensembl transcript: ENST00000534056
  gene symbol: FPGT
  hgvsc: ENST00000534056.1:c.965T>C
  hgvsp: ENSP00000432819.1:p.Met322Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000116783
  ensembl protein: ENSP00000359928
  ensembl transcript: ENST00000370891
  gene symbol: TNNI3K
  hgvsc: ENST00000370891.2:c.343+4364T>C
  variant of: http://identifiers.org/hgnc/19661
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000450895
  ensembl transcript: ENST00000557284
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000557284.2:c.382+4364T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359931
  ensembl transcript: ENST00000370894
  gene symbol: FPGT
  hgvsc: ENST00000370894.5:c.*400T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254685
  ensembl protein: ENSP00000359935
  ensembl transcript: ENST00000370898
  gene symbol: FPGT
  hgvsc: ENST00000370898.3:c.1766T>C
  hgvsp: ENSP00000359935.3:p.Met589Thr
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254685
  ensembl transcript: ENST00000524915
  gene symbol: FPGT
  hgvsc: ENST00000524915.1:n.448+1318T>C
  variant of: http://identifiers.org/hgnc/3825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359930
  ensembl transcript: ENST00000370893
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370893.1:c.343+4364T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359932
  ensembl transcript: ENST00000370895
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370895.1:c.343+4364T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000433587
  ensembl transcript: ENST00000534632
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000534632.1:c.343+4364T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl transcript: ENST00000533006
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000533006.1:n.369+4364T>C
  variant of: http://identifiers.org/hgnc/42952
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000259030
  ensembl protein: ENSP00000359936
  ensembl transcript: ENST00000370899
  gene symbol: FPGT-TNNI3K
  hgvsc: ENST00000370899.3:c.343+4364T>C
  variant of: http://identifiers.org/hgnc/42952
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met576Thr
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 403
bin: 9.75e1
variant carriers: 19

GenotypeDepth
all individuals: 420
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28190
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10111
bin: 9.75e1
variant carriers: 36

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7967
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

African
type: Population
allele count: 36
allele frequency: 3.459542571593312e-3
allele num: 10406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.599e0

FS
type: SiteQuality
SIO_000300: 1.836e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

DP
type: SiteQuality
SIO_000300: 1.982724e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

GenotypeDepth
all individuals: 5990
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3131
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4036
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

FS
type: SiteQuality
SIO_000300: 1.703e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.572e0

DP
type: SiteQuality
SIO_000300: 1.980256e6

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.331e1

GenotypeDepth
all individuals: 3821
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28203
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7970
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4036
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10085
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3395
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.98024e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.267e0

MQ
type: SiteQuality
SIO_000300: 6.061e1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

QD
type: SiteQuality
SIO_000300: 1.234e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.72e-1

GenotypeDepth
all individuals: 171
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10085
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
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GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 1.362e1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 9.360000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 1.9802e6

GenotypeDepth
all individuals: 187
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 2228
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7960
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.617e1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

FS
type: SiteQuality
SIO_000300: 1.349e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

DP
type: SiteQuality
SIO_000300: 1.980093e6

GenotypeDepth
all individuals: 187
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 818
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4039
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28140
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7958
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variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -8.934e-1

DP
type: SiteQuality
SIO_000300: 1.979929e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

QD
type: SiteQuality
SIO_000300: 1.458e1

MQRankSum
type: SiteQuality
SIO_000300: -7.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.589e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 421
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7959
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
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variant carriers: 0

GenotypeQuality
all individuals: 10083
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4041
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 28154
bin: 6.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.501e1

DP
type: SiteQuality
SIO_000300: 1.979794e6

BaseQRankSum
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SIO_000300: 2.69e0

InbreedingCoeff
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SIO_000300: 6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
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SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.535e-1

FS
type: SiteQuality
SIO_000300: 1.997e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.827e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10083
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 6.701e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.979709e6

QD
type: SiteQuality
SIO_000300: 1.469e1

GenotypeDepth
all individuals: 170
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

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

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

African
type: Population
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allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Other
type: Population
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allele num: 904
num of homozygotes: 0

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

DP
type: SiteQuality
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10083
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.681e0

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

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

East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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FS
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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FS
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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South Asian
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East Asian
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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African
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South Asian
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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DP
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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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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European (Non-Finnish)
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East Asian
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South Asian
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Latino
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African
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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BaseQRankSum
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QD
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VQSLOD
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DP
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ReadPosRankSum
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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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African
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South Asian
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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ReadPosRankSum
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FS
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MQ
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DP
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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East Asian
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South Asian
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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QD
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DP
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GenotypeQuality
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European (Finnish)
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FS
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MQ
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DP
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ReadPosRankSum
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SIO_000300: 8.83e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

GenotypeDepth
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 818
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10078
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4043
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.136e0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-2

DP
type: SiteQuality
SIO_000300: 1.979756e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.491e0

QD
type: SiteQuality
SIO_000300: 1.519e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeDepth
all individuals: 421
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28169
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.305e0

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.979827e6

GenotypeDepth
all individuals: 242
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 422
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1634
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10081
bin: 9.75e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28163
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7960
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4044
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 6.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.979979e6

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

QD
type: SiteQuality
SIO_000300: 1.168e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

GenotypeDepth
all individuals: 242
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28188
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3388
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4045
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7958
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.26e-1

QD
type: SiteQuality
SIO_000300: 1.519e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.980009e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.565e0

MQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.02e-1

GenotypeDepth
all individuals: 818
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variant carriers: 0

GenotypeDepth
all individuals: 324
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variant carriers: 0

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

GenotypeQuality
all individuals: 2231
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 28194
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7957
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4041
bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.746e0

MQ
type: SiteQuality
SIO_000300: 6.007e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.874e0

VQSLOD
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SIO_000300: 2.01e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.980132e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

DP
type: SiteQuality
SIO_000300: 1.980005e6

QD
type: SiteQuality
SIO_000300: 1.343e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 1.393e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

GenotypeDepth
all individuals: 389
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variant carriers: 8

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10088
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 4041
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028834504482675e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.993075331994364e-5
allele num: 66718
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

DP
type: SiteQuality
SIO_000300: 1.980821e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.605e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeDepth
all individuals: 170
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.99538355466291e-5
allele num: 66718
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.979973e6

ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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ClippingRankSum
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SIO_000300: 3.2e-2

VQSLOD
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FS
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SIO_000300: 1.731e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -7.6e-2

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 1.34e0

DP
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SIO_000300: 1.979643e6

BaseQRankSum
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SIO_000300: 8.799999999999999e-2

ReadPosRankSum
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MQ
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SIO_000300: 5.967e1

FS
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: -7.606000000000001e-1

MQRankSum
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SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.104e1

GenotypeDepth
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variant carriers: 20

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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variant carriers: 0

Latino
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allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

European (Finnish)
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allele count: 48
allele frequency: 7.259528130671506e-3
allele num: 6612
num of homozygotes: 0

African
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allele frequency: 3.846893633391037e-4
allele num: 10398
num of homozygotes: 0

Other
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 238
allele frequency: 3.567146282973621e-3
allele num: 66720
num of homozygotes: 0

MQ
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SIO_000300: 5.973e1

ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 2.001085e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 9.664e0

MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQ
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QD
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SIO_000300: 1.333e1

ClippingRankSum
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SIO_000300: 1.38e-1

DP
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GenotypeDepth
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66712
num of homozygotes: 0

Latino
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num of homozygotes: 0

InbreedingCoeff
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FS
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DP
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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SIO_000300: -7.04e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele count: 2
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allele num: 66712
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 5.014698253501643e-3
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European (Finnish)
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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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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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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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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South Asian
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East Asian
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MQRankSum
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VQSLOD
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DP
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FS
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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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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European (Non-Finnish)
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African
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East Asian
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South Asian
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European (Finnish)
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FS
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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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African
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num of homozygotes: 0

Latino
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allele frequency: 8.659508139937652e-5
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num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

Latino
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East Asian
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allele num: 8648
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European (Finnish)
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South Asian
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African
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Other
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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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 frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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FS
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VQSLOD
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QD
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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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: 1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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Other
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East Asian
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South Asian
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DP
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

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

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

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