11-1957402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957402
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957402
    reference: chr 11
allele count: 18
allele frequency: 1.507613447911955e-4
allele num: 119394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-42C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-42C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-42C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-791C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-791C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11785
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

11-1957407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957407
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957407
    reference: chr 11
allele count: 5
allele frequency: 4.187183867617995e-5
allele num: 119412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-37C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-37C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-37C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-786C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-786C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

11-1957408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957408
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957408
    reference: chr 11
allele count: 24
allele frequency: 2.009982915145221e-4
allele num: 119404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-36G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-36G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-785G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-36G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/11-1957418-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957418
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957418
    reference: chr 11
allele count: 1
allele frequency: 8.368761088608442e-6
allele num: 119492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-26C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-26C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-26C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-775C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-775C>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

11-1957419-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957419
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957419
    reference: chr 11
allele count: 1
allele frequency: 8.367780697203488e-6
allele num: 119506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-774C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-1957423-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957423
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957423
    reference: chr 11
allele count: 1
allele frequency: 8.366100560528738e-6
allele num: 119530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-21T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-21T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-770T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-21T>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-1957426-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957426
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957426
    reference: chr 11
allele count: 1
allele frequency: 8.36470096194061e-6
allele num: 119550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.664-18C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.625-18C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.658-18C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-767C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-767C>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

11-1957456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957456
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957456
    reference: chr 11
allele count: 2
allele frequency: 1.672492515595993e-5
allele num: 119582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.676C>T
  hgvsp: ENSP00000353815.3:p.Arg226Trp
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.670C>T
  hgvsp: ENSP00000370991.3:p.Arg224Trp
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.637C>T
  hgvsp: ENSP00000413203.1:p.Arg213Trp
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-737C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-737C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8517
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg224Trp
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

11-1957457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957457
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957457
    reference: chr 11
allele count: 2
allele frequency: 1.672436572842975e-5
allele num: 119586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.638G>A
  hgvsp: ENSP00000413203.1:p.Arg213Gln
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.671G>A
  hgvsp: ENSP00000370991.3:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.677G>A
  hgvsp: ENSP00000353815.3:p.Arg226Gln
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-736G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-736G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12049
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg224Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-1957462-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957462
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957462
    reference: chr 11
allele count: 93
allele frequency: 7.776960128445277e-4
allele num: 119584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.682A>C
  hgvsp: ENST00000360603.3:c.682A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.643A>C
  hgvsp: ENST00000446240.1:c.643A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.676A>C
  hgvsp: ENST00000381579.3:c.676A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-731A>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-731A>C
  variant of: http://identifiers.org/hgnc/11950
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 8491
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Arg226Arg
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-1957463-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957463
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957463
    reference: chr 11
allele count: 1
allele frequency: 8.362462577979963e-6
allele num: 119582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.677G>C
  hgvsp: ENSP00000370991.3:p.Arg226Thr
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.644G>C
  hgvsp: ENSP00000413203.1:p.Arg215Thr
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.683G>C
  hgvsp: ENSP00000353815.3:p.Arg228Thr
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-730G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-730G>C
  variant of: http://identifiers.org/hgnc/11950
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg226Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

11-1957473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957473
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957473
    reference: chr 11
allele count: 1
allele frequency: 8.364980844193866e-6
allele num: 119546
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.687G>A
  hgvsp: ENSP00000370991.3:p.Met229Ile
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.654G>A
  hgvsp: ENSP00000413203.1:p.Met218Ile
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.693G>A
  hgvsp: ENSP00000353815.3:p.Met231Ile
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-720G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-720G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12044
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met229Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-1957488-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957488
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957488
    reference: chr 11
allele count: 1
allele frequency: 8.369181326682624e-6
allele num: 119486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+4A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+4A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+4A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-705A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-705A>G
  variant of: http://identifiers.org/hgnc/11950
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12895
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.698+4A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

11-1957494-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957494
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957494
    reference: chr 11
allele count: 1
allele frequency: 8.373245805003851e-6
allele num: 119428
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+10C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+10C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+10C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-699C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-699C>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

11-1957494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957494
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957494
    reference: chr 11
allele count: 4
allele frequency: 3.34929832200154e-5
allele num: 119428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+10C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+10C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-699C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+10C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

11-1957495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957495
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957495
    reference: chr 11
allele count: 8
allele frequency: 6.698147962088483e-5
allele num: 119436
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-698G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

11-1957496-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957496
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957496
    reference: chr 11
allele count: 2
allele frequency: 1.67470525187567e-5
allele num: 119424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+12G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+12G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-697G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+12G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-697G>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

11-1957498-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957498
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957498
    reference: chr 11
allele count: 1
allele frequency: 8.372825158665037e-6
allele num: 119434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+14T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+14T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+14T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-695T>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-695T>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-1957500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957500
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957500
    reference: chr 11
allele count: 5
allele frequency: 4.187534547160014e-5
allele num: 119402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+16C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+16C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+16C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-693C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-693C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

11-1957511-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957511
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957511
    reference: chr 11
allele count: 1
allele frequency: 8.381948635418762e-6
allele num: 119304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+27A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+27A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+27A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-682A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-682A>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

11-1957516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957516
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957516
    reference: chr 11
allele count: 240
allele frequency: 2.012443609653021e-3
allele num: 119258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+32C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+32C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+32C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-677C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-677C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8470
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11854
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 4.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 5841
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 6.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
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: C
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-1957517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957517
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957517
    reference: chr 11
allele count: 16
allele frequency: 1.341539080710345e-4
allele num: 119266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-676G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-676G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12360
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-1957517-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957517
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957517
    reference: chr 11
allele count: 3
allele frequency: 2.515385776331897e-5
allele num: 119266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+33G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+33G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-676G>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+33G>C
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

11-1957525-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957525
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957525
    reference: chr 11
allele count: 1
allele frequency: 8.38841727342885e-6
allele num: 119212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+41G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+41G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+41G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-668G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-668G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-1957527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957527
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957527
    reference: chr 11
allele count: 3
allele frequency: 2.51724311534008e-5
allele num: 119178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+43G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+43G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-666G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+43G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-666G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-1957533-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957533
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957533
    reference: chr 11
allele count: 2
allele frequency: 1.67993817827504e-5
allele num: 119052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+49C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+49C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+49C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-660C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-660C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-1957534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957534
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957534
    reference: chr 11
allele count: 2
allele frequency: 1.681067814275628e-5
allele num: 118972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+50G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-659G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+50G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+50G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-659G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

11-1957534-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957534
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957534
    reference: chr 11
allele count: 5
allele frequency: 4.20266953568907e-5
allele num: 118972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+50G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+50G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-659G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+50G>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-1957535-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1957535
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1957535
    reference: chr 11
allele count: 25
allele frequency: 2.099605274208449e-4
allele num: 119070
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-658G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-658G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10898
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

11-1958142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958142
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958142
    reference: chr 11
allele count: 3
allele frequency: 5.534238488783943e-5
allele num: 54208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+658C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+658C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+658C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-51C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-51C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-1958151-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958151
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958151
    reference: chr 11
allele count: 1
allele frequency: 1.828420975645433e-5
allele num: 54692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+667G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+667G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+667G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-42G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-42G>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

11-1958156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958156
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958156
    reference: chr 11
allele count: 1
allele frequency: 1.800309653260361e-5
allele num: 55546
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+672T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-37T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+672T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+672T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-37T>C
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

11-1958157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958157
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958157
    reference: chr 11
allele count: 10
allele frequency: 1.814355178169679e-4
allele num: 55116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+673C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+673C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+673C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-36C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-36C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5770
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26249
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

11-1958158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958158
    reference: chr 11
allele count: 2
allele frequency: 3.585771658060814e-5
allele num: 55776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+674G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+674G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+674G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-35G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-35G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12792
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-1958163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958163
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958163
    reference: chr 11
allele count: 1
allele frequency: 1.748618591312863e-5
allele num: 57188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+679G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+679G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+679G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-30G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-30G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

11-1958165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958165
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958165
    reference: chr 11
allele count: 3
allele frequency: 5.199306759098787e-5
allele num: 57700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+681C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+681C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-28C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+681C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-28C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11785
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27071
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

11-1958166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958166
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958166
    reference: chr 11
allele count: 2
allele frequency: 3.442340791738382e-5
allele num: 58100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+682G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+682G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+682G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-27G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-1958166-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958166
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958166
    reference: chr 11
allele count: 1
allele frequency: 1.721170395869191e-5
allele num: 58100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+682G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+682G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+682G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-27G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-27G>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

11-1958170-TGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958168
    reference: chr 11
allele count: 41
allele frequency: 6.820601543784935e-4
allele num: 60112
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-21_682-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-21_676-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-21_658-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+688_665+689delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-21_625-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-21_658-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-21_640-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-21_643-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+688_704+689delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-21_691-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-21_688-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+688_698+689delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-21_691-20delAG
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-21_715-20delAG
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10040
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8643
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: TGA
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-1958179-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958179
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958179
    reference: chr 11
allele count: 1
allele frequency: 1.563672754565924e-5
allele num: 63952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+695C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+695C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+695C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-14C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-14C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

11-1958180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958180
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958180
    reference: chr 11
allele count: 1
allele frequency: 1.54669471339747e-5
allele num: 64654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+696A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+696A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+696A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-13A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-13A>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-1958181-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958181
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958181
    reference: chr 11
allele count: 1
allele frequency: 1.53907716932927e-5
allele num: 64974
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+697T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+697T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-12T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+697T>C
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-12T>C
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

11-1958182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958182
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958182
    reference: chr 11
allele count: 2
allele frequency: 3.070970119460738e-5
allele num: 65126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+698G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-11G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-11G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

11-1958191-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958191
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958191
    reference: chr 11
allele count: 1
allele frequency: 1.466920932961713e-5
allele num: 68170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.691-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.640-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+707A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.676-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.682-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+707A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.625-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.658-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.658-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.643-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.688-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.691-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.715-2A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+707A>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.682-2A>G
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

11-1958200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958200
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958200
    reference: chr 11
allele count: 2
allele frequency: 2.889839324933534e-5
allele num: 69208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.665C>T
  hgvsp: ENSP00000370970.1:p.Thr222Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.722C>T
  hgvsp: ENSP00000380468.1:p.Thr241Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.632C>T
  hgvsp: ENSP00000380471.2:p.Thr211Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.695C>T
  hgvsp: ENSP00000370960.3:p.Thr232Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+716C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.647C>T
  hgvsp: ENSP00000370969.2:p.Thr216Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+716C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.689C>T
  hgvsp: ENSP00000278317.6:p.Thr230Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.650C>T
  hgvsp: ENSP00000344870.4:p.Thr217Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.698C>T
  hgvsp: ENSP00000370973.4:p.Thr233Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.683C>T
  hgvsp: ENSP00000371001.3:p.Thr228Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.698C>T
  hgvsp: ENSP00000370975.4:p.Thr233Met
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+716C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.665C>T
  hgvsp: ENSP00000370961.3:p.Thr222Met
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23862
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr230Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ

11-1958201-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958201
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958201
    reference: chr 11
allele count: 2
allele frequency: 2.883672645481285e-5
allele num: 69356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+717G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.699G>A
  hgvsp: ENST00000381563.4:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.684G>A
  hgvsp: ENST00000381589.3:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.648G>A
  hgvsp: ENST00000381557.2:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.723G>A
  hgvsp: ENST00000397301.1:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.666G>A
  hgvsp: ENST00000381549.3:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.690G>A
  hgvsp: ENST00000278317.6:c.690G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.699G>A
  hgvsp: ENST00000381561.4:c.699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.696G>A
  hgvsp: ENST00000381548.3:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.666G>A
  hgvsp: ENST00000381558.1:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.633G>A
  hgvsp: ENST00000397304.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.651G>A
  hgvsp: ENST00000344578.4:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+717G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+717G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15421
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr230Thr
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

11-1958202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958202
    reference: chr 11
allele count: 3
allele frequency: 4.30786904078116e-5
allele num: 69640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.634C>T
  hgvsp: ENSP00000380471.2:p.Leu212Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.649C>T
  hgvsp: ENSP00000370969.2:p.Leu217Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+718C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.697C>T
  hgvsp: ENSP00000370960.3:p.Leu233Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.691C>T
  hgvsp: ENSP00000278317.6:p.Leu231Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.685C>T
  hgvsp: ENSP00000371001.3:p.Leu229Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+718C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.700C>T
  hgvsp: ENSP00000370973.4:p.Leu234Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.724C>T
  hgvsp: ENSP00000380468.1:p.Leu242Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.652C>T
  hgvsp: ENSP00000344870.4:p.Leu218Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.667C>T
  hgvsp: ENSP00000370961.3:p.Leu223Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.700C>T
  hgvsp: ENSP00000370975.4:p.Leu234Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.667C>T
  hgvsp: ENSP00000370970.1:p.Leu223Phe
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+718C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15431
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu231Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

11-1958209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958209
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958209
    reference: chr 11
allele count: 40
allele frequency: 5.711837783806939e-4
allele num: 70030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+725G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.704G>A
  hgvsp: ENSP00000370960.3:p.Ser235Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+725G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.659G>A
  hgvsp: ENSP00000344870.4:p.Ser220Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.731G>A
  hgvsp: ENSP00000380468.1:p.Ser244Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.707G>A
  hgvsp: ENSP00000370973.4:p.Ser236Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.698G>A
  hgvsp: ENSP00000278317.6:p.Ser233Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+725G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.707G>A
  hgvsp: ENSP00000370975.4:p.Ser236Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.674G>A
  hgvsp: ENSP00000370961.3:p.Ser225Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.656G>A
  hgvsp: ENSP00000370969.2:p.Ser219Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.641G>A
  hgvsp: ENSP00000380471.2:p.Ser214Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.692G>A
  hgvsp: ENSP00000371001.3:p.Ser231Asn
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.674G>A
  hgvsp: ENSP00000370970.1:p.Ser225Asn
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14966
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 23453
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser233Asn
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-1958212-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958212
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958212
    reference: chr 11
allele count: 4
allele frequency: 5.771006463527239e-5
allele num: 69312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.677G>A
  hgvsp: ENSP00000370970.1:p.Arg226His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.734G>A
  hgvsp: ENSP00000380468.1:p.Arg245His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.695G>A
  hgvsp: ENSP00000371001.3:p.Arg232His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+728G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+728G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.662G>A
  hgvsp: ENSP00000344870.4:p.Arg221His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.707G>A
  hgvsp: ENSP00000370960.3:p.Arg236His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.659G>A
  hgvsp: ENSP00000370969.2:p.Arg220His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.644G>A
  hgvsp: ENSP00000380471.2:p.Arg215His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.701G>A
  hgvsp: ENSP00000278317.6:p.Arg234His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.710G>A
  hgvsp: ENSP00000370975.4:p.Arg237His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+728G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.677G>A
  hgvsp: ENSP00000370961.3:p.Arg226His
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.710G>A
  hgvsp: ENSP00000370973.4:p.Arg237His
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13997
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg234His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

11-1958236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958236
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958236
    reference: chr 11
allele count: 4
allele frequency: 6.584145377929945e-5
allele num: 60752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+752G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+752G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+3G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+752G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23556
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15209
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.722+3G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

11-1958238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958238
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958238
    reference: chr 11
allele count: 2
allele frequency: 3.312245371137094e-5
allele num: 60382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+754G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+754G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+754G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+5G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+5G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15285
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.722+5G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-1958246-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958246
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958245
    reference: chr 11
allele count: 1
allele frequency: 1.828354115625114e-5
allele num: 54694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+764delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+764delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+764delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+15delC
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+15delC
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: GC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/11-1958248-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958248
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958248
    reference: chr 11
allele count: 12
allele frequency: 2.242822966507177e-4
allele num: 53504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+764C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+764C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+15C>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+764C>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22375
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

11-1958248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958248
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958248
    reference: chr 11
allele count: 8
allele frequency: 1.495215311004785e-4
allele num: 53504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+764C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+764C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+764C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+15C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+15C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22375
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-1958249-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958249
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958249
    reference: chr 11
allele count: 1
allele frequency: 1.875328182431926e-5
allele num: 53324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+765G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+765G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+765G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+16G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+16G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22379
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

11-1958255-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958255
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958255
    reference: chr 11
allele count: 5
allele frequency: 1.092657342657343e-4
allele num: 45760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+771G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+771G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+22G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+771G>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+22G>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22730
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

11-1958256-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958256
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958256
    reference: chr 11
allele count: 1
allele frequency: 2.171835635479107e-5
allele num: 46044
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+772C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+772C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+772C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+23C>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+23C>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-1958256-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958256
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958256
    reference: chr 11
allele count: 1
allele frequency: 2.171835635479107e-5
allele num: 46044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+772C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+23C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+772C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+772C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+23C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

11-1958258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958258
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958258
    reference: chr 11
allele count: 1
allele frequency: 2.274588299517787e-5
allele num: 43964
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+774C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+25C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+25C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-1958259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958259
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958259
    reference: chr 11
allele count: 3
allele frequency: 6.848376934666484e-5
allele num: 43806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+775C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+775C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+26C>T
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+775C>T
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23077
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-1958260-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958260
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958260
    reference: chr 11
allele count: 10
allele frequency: 2.382881380164895e-4
allele num: 41966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+776G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+27G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+776G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+776G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23267
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-1958262-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958262
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958262
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 41578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+778A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+778A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+778A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+29A>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+29A>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23386
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

11-1958266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958266
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958266
    reference: chr 11
allele count: 1
allele frequency: 2.56278831368529e-5
allele num: 39020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+782G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+782G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+782G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+33G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+33G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23709
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

11-1958280-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958280
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958280
    reference: chr 11
allele count: 3
allele frequency: 9.707481232202951e-5
allele num: 30904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+796T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+796T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+47T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+796T>G
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+47T>G
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-1958284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1958284
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 1958284
    reference: chr 11
allele count: 2
allele frequency: 6.80133306128001e-5
allele num: 29406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370973
  ensembl transcript: ENST00000381561
  gene symbol: TNNT3
  hgvsc: ENST00000381561.4:c.731+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000353815
  ensembl transcript: ENST00000360603
  gene symbol: TNNT3
  hgvsc: ENST00000360603.3:c.704+800G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370975
  ensembl transcript: ENST00000381563
  gene symbol: TNNT3
  hgvsc: ENST00000381563.4:c.731+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380471
  ensembl transcript: ENST00000397304
  gene symbol: TNNT3
  hgvsc: ENST00000397304.2:c.665+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000380468
  ensembl transcript: ENST00000397301
  gene symbol: TNNT3
  hgvsc: ENST00000397301.1:c.755+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000344870
  ensembl transcript: ENST00000344578
  gene symbol: TNNT3
  hgvsc: ENST00000344578.4:c.683+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370961
  ensembl transcript: ENST00000381549
  gene symbol: TNNT3
  hgvsc: ENST00000381549.3:c.698+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000371001
  ensembl transcript: ENST00000381589
  gene symbol: TNNT3
  hgvsc: ENST00000381589.3:c.716+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370960
  ensembl transcript: ENST00000381548
  gene symbol: TNNT3
  hgvsc: ENST00000381548.3:c.728+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000278317
  ensembl transcript: ENST00000278317
  gene symbol: TNNT3
  hgvsc: ENST00000278317.6:c.722+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370970
  ensembl transcript: ENST00000381558
  gene symbol: TNNT3
  hgvsc: ENST00000381558.1:c.698+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370969
  ensembl transcript: ENST00000381557
  gene symbol: TNNT3
  hgvsc: ENST00000381557.2:c.680+51G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000413203
  ensembl transcript: ENST00000446240
  gene symbol: TNNT3
  hgvsc: ENST00000446240.1:c.665+800G>A
  variant of: http://identifiers.org/hgnc/11950
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130595
  ensembl protein: ENSP00000370991
  ensembl transcript: ENST00000381579
  gene symbol: TNNT3
  hgvsc: ENST00000381579.3:c.698+800G>A
  variant of: http://identifiers.org/hgnc/11950
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24995
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14764
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

GenotypeDepth
all individuals: 923
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 12126
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 2443
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8469
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4459
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6516
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4951
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19207
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 3396
bin: 7.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

African
type: Population
allele count: 18
allele frequency: 1.869158878504673e-3
allele num: 9630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65692
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.378e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

DP
type: SiteQuality
SIO_000300: 2.25375e6

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

FS
type: SiteQuality
SIO_000300: 7.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeDepth
all individuals: 899
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2444
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4499
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4956
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19199
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14015
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.610350076103501e-5
allele num: 65700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 2.260859e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

GenotypeDepth
all individuals: 1643
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 899
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8504
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 2445
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 925
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4955
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19211
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 230
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.58751902587519e-4
allele num: 65700
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.607335303320007e-4
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.037990450487856e-4
allele num: 9634
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

FS
type: SiteQuality
SIO_000300: 1.639e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

DP
type: SiteQuality
SIO_000300: 2.262977e6

GenotypeDepth
all individuals: 7243
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 923
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2445
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19203
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4513
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520866285436184e-5
allele num: 65752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.518e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 9.17e0

DP
type: SiteQuality
SIO_000300: 2.268538e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.763e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 720
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5781
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6695
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19202
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65762
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.597e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 2.269023e6

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 8.94e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

GenotypeDepth
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1643
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 899
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19202
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3455
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6586
num of homozygotes: 0

Latino
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South Asian
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.519941634241245e-5
allele num: 65792
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 2.6e-3

ClippingRankSum
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SIO_000300: 4.92e-1

BaseQRankSum
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SIO_000300: -1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -8.43e-1

QD
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SIO_000300: 1.062e1

FS
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.68e-1

ReadPosRankSum
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SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.270624e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.520265134239411e-5
allele num: 65778
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 2.26678e6

MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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QD
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SIO_000300: 1.046e1

ReadPosRankSum
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SIO_000300: 1.44e0

MQRankSum
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SIO_000300: 1.28e0

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

African
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allele count: 1
allele frequency: 1.038853106170787e-4
allele num: 9626
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65738
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 3.6e-2

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.6e-3

VQSLOD
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QD
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MQRankSum
type: SiteQuality
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DP
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SIO_000300: 2.264366e6

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 2.085e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521190179196203e-5
allele num: 65738
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 2.077706212341575e-4
allele num: 9626
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 4.6e-3

FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.022e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 2.264366e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.038853106170787e-4
allele num: 9626
num of homozygotes: 0

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

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

South Asian
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allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.084020320627871e-5
allele num: 65746
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QD
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.042195248091022e-5
allele num: 65742
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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DP
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.520958812435359e-5
allele num: 65748
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.486750348675035e-4
allele num: 8604
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521236460995497e-5
allele num: 65736
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -9.46e-1

DP
type: SiteQuality
SIO_000300: 2.261735e6

FS
type: SiteQuality
SIO_000300: 6.63e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.22e0

VQSLOD
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SIO_000300: 2.48e0

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65676
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 5.8e-1

DP
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MQRankSum
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QD
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InbreedingCoeff
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FS
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SIO_000300: 2.937e0

BaseQRankSum
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SIO_000300: 1.48e0

ReadPosRankSum
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SIO_000300: 2.09e0

ClippingRankSum
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SIO_000300: -6.65e-1

MQ
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SIO_000300: 5.967e1

GenotypeDepth
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variant carriers: 21

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 25

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 1
allele frequency: 1.16333178222429e-4
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
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allele count: 143
allele frequency: 2.17808511286441e-3
allele num: 65654
num of homozygotes: 0

European (Finnish)
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allele count: 94
allele frequency: 1.435991445157348e-2
allele num: 6546
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 2.7e-1

QD
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 7.82e-1

InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 3.02e0

ClippingRankSum
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SIO_000300: 6.8e-2

VQSLOD
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SIO_000300: 4.31e0

DP
type: SiteQuality
SIO_000300: 2.253569e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 16

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 15
allele frequency: 9.096422073984233e-4
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522858100082234e-5
allele num: 65666
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

VQSLOD
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ClippingRankSum
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SIO_000300: 6.5e-2

MQRankSum
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DP
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SIO_000300: 2.250635e6

BaseQRankSum
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SIO_000300: -2.519e0

QD
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SIO_000300: 1.447e1

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 1.819284414796847e-4
allele num: 16490
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European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

Other
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
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BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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ClippingRankSum
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FS
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.048966400390268e-5
allele num: 65596
num of homozygotes: 0

Other
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South Asian
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allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

East Asian
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Latino
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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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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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65524
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Latino
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allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 1.044277360066834e-4
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 5
allele frequency: 5.816658911121452e-4
allele num: 8596
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele num: 11470
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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allele frequency: 2.293577981651376e-3
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Latino
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Other
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African
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European (Non-Finnish)
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1252
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.270111183780248e-5
allele num: 30580
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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SIO_000300: 1.69e0

FS
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SIO_000300: 1.664e0

DP
type: SiteQuality
SIO_000300: 1.181477e6

QD
type: SiteQuality
SIO_000300: 1.256e1

ClippingRankSum
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 2

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

African
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allele count: 8
allele frequency: 1.470047776552738e-3
allele num: 5442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3408
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1262
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 6.597611664577422e-5
allele num: 30314
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

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

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

African
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allele count: 2
allele frequency: 3.644314868804665e-4
allele num: 5488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30758
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3482
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1270
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -1.133e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

FS
type: SiteQuality
SIO_000300: 1.0249e1

ClippingRankSum
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SIO_000300: -9.1e-2

VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.167e1

ReadPosRankSum
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

DP
type: SiteQuality
SIO_000300: 1.193557e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5576
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 2.75330396475771e-4
allele num: 3632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1332
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.213409e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ReadPosRankSum
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SIO_000300: 5.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.94e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3676
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31904
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 9.589566551591868e-5
allele num: 10428
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4322
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

African
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allele count: 2
allele frequency: 3.566333808844508e-4
allele num: 5608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 7.27e-1

FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
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South Asian
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allele frequency: 9.554748710108924e-5
allele num: 10466
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 3710
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
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East Asian
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allele num: 4370
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QD
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MQRankSum
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MQ
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ClippingRankSum
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DP
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32152
num of homozygotes: 0

Latino
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: 400
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African
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele count: 1
allele frequency: 2.288329519450801e-4
allele num: 4370
num of homozygotes: 0

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

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

GenotypeDepth
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variant carriers: 27

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

European (Non-Finnish)
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allele num: 33436
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African
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East Asian
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South Asian
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Other
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Latino
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 35726
num of homozygotes: 0

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

African
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European (Non-Finnish)
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num of homozygotes: 0

Latino
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South Asian
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European (Finnish)
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Other
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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South Asian
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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European (Finnish)
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MQRankSum
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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FS
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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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African
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European (Non-Finnish)
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East Asian
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.629999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

FS
type: SiteQuality
SIO_000300: 2.687e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

DP
type: SiteQuality
SIO_000300: 1.372508e6

QD
type: SiteQuality
SIO_000300: 5.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 6472
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 2
allele frequency: 1.778410101369376e-4
allele num: 11246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

QD
type: SiteQuality
SIO_000300: 1.671e1

VQSLOD
type: SiteQuality
SIO_000300: -4.612e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.375312e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5352
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.137747097583935e-4
allele num: 6374
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.925298421255295e-4
allele num: 5194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

DP
type: SiteQuality
SIO_000300: 1.374767e6

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

FS
type: SiteQuality
SIO_000300: 5.739e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e-1

GenotypeDepth
all individuals: 282
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variant carriers: 0

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 15

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 37

GenotypeQuality
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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: 1382
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1924
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

Latino
type: Population
allele count: 40
allele frequency: 7.564296520423601e-3
allele num: 5288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39260
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

DP
type: SiteQuality
SIO_000300: 1.374767e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.352e0

FS
type: SiteQuality
SIO_000300: 1.105e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 9.66e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.739538723492079e-5
allele num: 38762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5180
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5338
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 5.230125523012552e-4
allele num: 1912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 6.7e-3

MQRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33464
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 4
allele frequency: 9.263547938860583e-4
allele num: 4318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1522
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QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

BaseQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 1.02e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.677268475210477e-4
allele num: 4276
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 428
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.657e0

VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.48e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

DP
type: SiteQuality
SIO_000300: 1.203761e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.340906053721769e-5
allele num: 29932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

FS
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SIO_000300: 8.422000000000001e0

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 5.78e0

ReadPosRankSum
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SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e-1

DP
type: SiteQuality
SIO_000300: 1.141267e6

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 142
bin: 8.25e1
variant carriers: 0

African
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allele count: 11
allele frequency: 2.091254752851711e-3
allele num: 5260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.425361375625129e-5
allele num: 29194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.19e-2

DP
type: SiteQuality
SIO_000300: 1.130811e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9

GenotypeQuality
all individuals: 723
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.901140684410646e-4
allele num: 5260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.850722751250257e-5
allele num: 29194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 1.453488372093023e-3
allele num: 3440
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.475e1

FS
type: SiteQuality
SIO_000300: 6.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.19e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 1.130811e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.439499208915182e-5
allele num: 29074
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3424
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.35e-1

QD
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SIO_000300: 2.174e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

BaseQRankSum
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SIO_000300: -7.2e-1

DP
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SIO_000300: 1.129336e6

InbreedingCoeff
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SIO_000300: -2.34e-2

MQRankSum
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 3.337e0

VQSLOD
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SIO_000300: -1.548e0

GenotypeDepth
all individuals: 382
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variant carriers: 0

GenotypeDepth
all individuals: 281
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3272
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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: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.63025758069775e-4
allele num: 24536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4762
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.035411058190101e-4
allele num: 9658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2528
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.95e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 7.19e0

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.080859e6

BaseQRankSum
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SIO_000300: -1.38e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 25
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.04236397445226e-5
allele num: 24738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3196
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.079347e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: 1.0e0

FS
type: SiteQuality
SIO_000300: 1.232e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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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: 1.25e1
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GenotypeQuality
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bin: 9.75e1
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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
all individuals: 3487
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.25e1
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 4.04236397445226e-5
allele num: 24738
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 4.257855743847399e-5
allele num: 23486
num of homozygotes: 0

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

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

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

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

DP
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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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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.493e0

InbreedingCoeff
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SIO_000300: 2.63e-2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.41306266548985e-4
allele num: 2266
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.170138888888889e-4
allele num: 4608
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 4.275331338178709e-5
allele num: 23390
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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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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SIO_000300: -5.77e-1

DP
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SIO_000300: 1.065018e6

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

European (Non-Finnish)
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allele count: 10
allele frequency: 4.486316733961418e-4
allele num: 22290
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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SIO_000300: -1.468e0

ReadPosRankSum
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SIO_000300: 2.27e-1

DP
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SIO_000300: 1.05559e6

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22076
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele count: 0
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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African
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allele frequency: 9.052504526252263e-4
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FS
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 6448
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8366
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6378
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5980
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9625
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 547
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.385233411829893e-4
allele num: 14438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8844
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: -1.024e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1