5-33453355-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453355
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453355
    reference: chr 5
allele count: 1
allele frequency: 1.123620755522596e-5
allele num: 88998
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1732A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1732A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-44A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-39A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13916
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

5-33453356-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453356
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453356
    reference: chr 5
allele count: 2
allele frequency: 2.222913795403014e-5
allele num: 89972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1731T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-43T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-38T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1731T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

5-33453357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453357
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453357
    reference: chr 5
allele count: 2
allele frequency: 2.231893761856936e-5
allele num: 89610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1730A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-37A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1730A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-37A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14668
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

5-33453361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453361
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453361
    reference: chr 5
allele count: 1
allele frequency: 1.100352112676056e-5
allele num: 90880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1726G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-38G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1726G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-33G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

5-33453365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453365
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453365
    reference: chr 5
allele count: 16
allele frequency: 1.737921445950643e-4
allele num: 92064
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1722G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1722G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-29G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-34G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9551
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9248
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19632
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

5-33453366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453366
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453366
    reference: chr 5
allele count: 1
allele frequency: 1.111901796833304e-5
allele num: 89936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1721G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1721G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-33G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-28G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-28G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18639
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/5-33453367-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453367
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
allele count: 1421
allele frequency: 1.68997668997669e-2
allele num: 84084
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-31dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1719dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1719dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-26dupC
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-26dupC
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 3.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 7.5e0
  variant carriers: 294
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 2.75e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 9932
  bin: 1.25e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.5e0
  variant carriers: 341
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 1.75e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 194
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

5-33453367-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453367
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453367
    reference: chr 5
allele count: 529
allele frequency: 6.291327719899148e-3
allele num: 84084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1720A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-32A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1720A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-27A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-27A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 1.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 9932
  bin: 1.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 2.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 3.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
num of homozygotes: 4
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

5-33453368-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453367
    reference: chr 5
allele count: 2544
allele frequency: 1.32693511370749e-1
allele num: 19172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1697delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1697delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-9delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-4delT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-4delT
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 1.25e1
  variant carriers: 1897
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 782
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 2636
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 62
genotype quality: GenotypeQuality
num of homozygotes: 6
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CT
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

5-33453368-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453366
    reference: chr 5
allele count: 2817
allele frequency: 1.469330273315251e-1
allele num: 19172
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 485
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 1004
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 1.25e1
  variant carriers: 1736
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 1122
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 1.25e1
  variant carriers: 241
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 6.75e1
  variant carriers: 298
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 6.25e1
  variant carriers: 282
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.75e1
  variant carriers: 203
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 5.75e1
  variant carriers: 261
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 224
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 8.25e1
  variant carriers: 215
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 7.25e1
  variant carriers: 229
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 4.75e1
  variant carriers: 219
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 220
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 7.5e0
  variant carriers: 248
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 2.25e1
  variant carriers: 230
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 1.75e1
  variant carriers: 257
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 138
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 2.75e1
  variant carriers: 212
genotype quality: GenotypeQuality
  all individuals: 33138
  bin: 2.5e0
  variant carriers: 253
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 4.25e1
  variant carriers: 200
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 5.25e1
  variant carriers: 242
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 161
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 424
num of homozygotes: 0
population: African
  type: Population
  allele count: 216
  allele frequency: 1.330049261083744e-1
  allele num: 1624
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 357
  allele frequency: 1.952954048140044e-1
  allele num: 1828
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 98
  allele frequency: 9.333333333333334e-2
  allele num: 1050
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 86
  allele frequency: 9.492273730684327e-2
  allele num: 906
  num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: CTT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

5-33453368-CTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453365
    reference: chr 5
allele count: 1252
allele frequency: 6.530356770290006e-2
allele num: 19172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-6_330-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-11_330-9delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-6_330-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-6_18-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-6_330-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-6_*287-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-6_*283-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-6_429-4delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1699_128-1697delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1699_330-1697delTTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-6_139-4delTTT
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 274
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 1.25e1
  variant carriers: 526
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 464
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: CTTT
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

5-33453368-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453369
    reference: chr 5
allele count: 261
allele frequency: 1.361360317129147e-2
allele num: 19172
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1697dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1697dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-4dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-9dupT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-4dupT
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 556
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 1.25e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

5-33453368-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453370
    reference: chr 5
allele count: 51
allele frequency: 2.660129355309827e-3
allele num: 19172
alternate allele: CTT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-5_139-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-5_330-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-10_330-9dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-5_18-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-5_330-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-5_*287-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-5_330-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1698_330-1697dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-5_429-4dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1698_128-1697dupTT
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-5_*283-4dupTT
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 1.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

5-33453368-CTTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453368
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453364
    reference: chr 5
allele count: 230
allele frequency: 1.199666179845608e-2
allele num: 19172
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 1.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 2.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8538
  bin: 1.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 8.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 1.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 1.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 33138
  bin: 2.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 2.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 2.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 5.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 66
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 7.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 4.75e1
  variant carriers: 14
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 5
  allele frequency: 5.518763796909493e-3
  allele num: 906
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 58
  allele frequency: 1.899148657498363e-2
  allele num: 3054
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 117
  allele frequency: 1.113013698630137e-2
  allele num: 10512
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 16
  allele frequency: 8.752735229759299e-3
  allele num: 1828
  num of homozygotes: 0
population: African
population: Latino
population: Other
reference allele: CTTTT
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

5-33453369-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453369
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453369
    reference: chr 5
allele count: 314
allele frequency: 3.272196748645269e-2
allele num: 9596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-30T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1718T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-25T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1718T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 1.25e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 7003
  bin: 1.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 2.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 2.5e0
  variant carriers: 253
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.5e0
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 2.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
num of homozygotes: 19
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

5-33453370-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453370
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453370
    reference: chr 5
allele count: 85
allele frequency: 4.857142857142857e-2
allele num: 1750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1717T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-29T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1717T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-24T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-24T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 1.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 1.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

5-33453371-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453371
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453371
    reference: chr 5
allele count: 41
allele frequency: 9.313948205361199e-3
allele num: 4402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-28T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-23T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1716T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1716T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-23T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 1.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 8944
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7738
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

5-33453372-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453372
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453372
    reference: chr 5
allele count: 10
allele frequency: 8.039877793857533e-4
allele num: 12438
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1715T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-27T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-22T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1715T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

5-33453390-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453390
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453390
    reference: chr 5
allele count: 3
allele frequency: 2.635879593020191e-5
allele num: 113814
alternate allele: A
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 3
  allele frequency: 3.282275711159737e-4
  allele num: 9140
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8020
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10966
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 16010
  num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

5-33453390-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453390
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453391
    reference: chr 5
allele count: 1
allele frequency: 8.786265310067303e-6
allele num: 113814
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-7dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1695dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-2dupA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1695dupA
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.429-2dupA
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

5-33453390-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453390
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453389
    reference: chr 5
allele count: 2
allele frequency: 1.757253062013461e-5
allele num: 113814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-7delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-2delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1695delA
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1695delA
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.429-2delA
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: TA
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

5-33453391-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453391
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453391
    reference: chr 5
allele count: 1
allele frequency: 9.611872585017014e-6
allele num: 104038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1696A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1696A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-3A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-8A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-3A>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.429-3A>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

5-33453392-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453392
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453392
    reference: chr 5
allele count: 1
allele frequency: 8.615787569141696e-6
allele num: 116066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1695A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-7A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1695A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-2A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-2A>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11401
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.429-2A>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

5-33453393-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453393
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453393
    reference: chr 5
allele count: 1
allele frequency: 8.578830876928093e-6
allele num: 116566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.18-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.330-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.429-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.330-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-6G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.330-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1694G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*283-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.139-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*287-1G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1694G>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12124
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.429-1G>T
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

5-33453397-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453397
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453397
    reference: chr 5
allele count: 3
allele frequency: 2.530407058148754e-5
allele num: 118558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*290A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.21A>G
  hgvsp: ENST00000541634.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.333A>G
  hgvsp: ENST00000514259.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.330-2A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.142A>G
  hgvsp: ENSP00000427627.1:p.Arg48Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1690A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1690A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.333A>G
  hgvsp: ENST00000502553.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*286A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.333A>G
  hgvsp: ENST00000265112.3:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.432A>G
  hgvsp: ENST00000455217.2:c.432A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.330-2A>G
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/5-33453400-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453400
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453400
    reference: chr 5
allele count: 2
allele frequency: 1.682255568265931e-5
allele num: 118888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.331C>A
  hgvsp: ENSP00000422291.1:p.Pro111Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.336C>A
  hgvsp: ENST00000514259.1:c.336C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1687C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1687C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.24C>A
  hgvsp: ENST00000541634.1:c.24C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.145C>A
  hgvsp: ENSP00000427627.1:p.Pro49Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.336C>A
  hgvsp: ENST00000502553.1:c.336C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.435C>A
  hgvsp: ENST00000455217.2:c.435C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*289C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.336C>A
  hgvsp: ENST00000265112.3:c.336C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*293C>A
  variant of: http://identifiers.org/hgnc/11572
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro49Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

5-33453405-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453405
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453405
    reference: chr 5
allele count: 1
allele frequency: 8.39390937935434e-6
allele num: 119134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.341C>T
  hgvsp: ENSP00000422130.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.440C>T
  hgvsp: ENSP00000387710.2:p.Ala147Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.341C>T
  hgvsp: ENSP00000265112.3:p.Ala114Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1682C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.341C>T
  hgvsp: ENSP00000424387.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*298C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*294C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.336C>T
  hgvsp: ENST00000505012.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1682C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.150C>T
  hgvsp: ENST00000508361.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.29C>T
  hgvsp: ENSP00000438469.1:p.Ala10Val
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala147Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

5-33453406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453406
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453406
    reference: chr 5
allele count: 1
allele frequency: 8.390106386548982e-6
allele num: 119188
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.441C>T
  hgvsp: ENST00000455217.2:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.151C>T
  hgvsp: ENSP00000427627.1:p.Arg51Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*299C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.342C>T
  hgvsp: ENST00000514259.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.342C>T
  hgvsp: ENST00000502553.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.30C>T
  hgvsp: ENST00000541634.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.342C>T
  hgvsp: ENST00000265112.3:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.337C>T
  hgvsp: ENSP00000422291.1:p.Arg113Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*295C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1681C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1681C>T
  variant of: http://identifiers.org/hgnc/11572
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg51Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

5-33453407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453407
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453407
    reference: chr 5
allele count: 157
allele frequency: 1.3174456658555e-3
allele num: 119170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.152G>A
  hgvsp: ENSP00000427627.1:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.31G>A
  hgvsp: ENSP00000438469.1:p.Asp11Asn
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1680G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*300G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.338G>A
  hgvsp: ENSP00000422291.1:p.Arg113Gln
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*296G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.442G>A
  hgvsp: ENSP00000387710.2:p.Asp148Asn
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.343G>A
  hgvsp: ENSP00000424387.1:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.343G>A
  hgvsp: ENSP00000422130.1:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1680G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.343G>A
  hgvsp: ENSP00000265112.3:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12978
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12884
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 7778
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
hgvs: p.Asp148Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

5-33453413-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453413
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453413
    reference: chr 5
allele count: 1
allele frequency: 8.384056877441857e-6
allele num: 119274
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.448A>G
  hgvsp: ENSP00000387710.2:p.Thr150Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.158A>G
  hgvsp: ENSP00000427627.1:p.His53Arg
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.344A>G
  hgvsp: ENSP00000422291.1:p.His115Arg
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*306A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.349A>G
  hgvsp: ENSP00000265112.3:p.Thr117Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.37A>G
  hgvsp: ENSP00000438469.1:p.Thr13Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.349A>G
  hgvsp: ENSP00000422130.1:p.Thr117Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*302A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.349A>G
  hgvsp: ENSP00000424387.1:p.Thr117Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1674A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1674A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr150Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

5-33453415-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453415
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453415
    reference: chr 5
allele count: 1
allele frequency: 8.35282325425994e-6
allele num: 119720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.346C>T
  hgvsp: ENSP00000422291.1:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*304C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.351C>T
  hgvsp: ENST00000514259.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.351C>T
  hgvsp: ENST00000265112.3:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.160C>T
  hgvsp: ENSP00000427627.1:p.Arg54Cys
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1672C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1672C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.351C>T
  hgvsp: ENST00000502553.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.450C>T
  hgvsp: ENST00000455217.2:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.39C>T
  hgvsp: ENST00000541634.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*308C>T
  variant of: http://identifiers.org/hgnc/11572
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg54Cys
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum

5-33453416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453416
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453416
    reference: chr 5
allele count: 208
allele frequency: 1.736545943328491e-3
allele num: 119778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1671G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*305G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.40G>A
  hgvsp: ENSP00000438469.1:p.Val14Ile
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.347G>A
  hgvsp: ENSP00000422291.1:p.Arg116His
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.451G>A
  hgvsp: ENSP00000387710.2:p.Val151Ile
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.352G>A
  hgvsp: ENSP00000265112.3:p.Val118Ile
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*309G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.161G>A
  hgvsp: ENSP00000427627.1:p.Arg54His
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1671G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.352G>A
  hgvsp: ENSP00000424387.1:p.Val118Ile
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.352G>A
  hgvsp: ENSP00000422130.1:p.Val118Ile
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13862
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Val151Ile
num of homozygotes: 1
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

5-33453420-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453420
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453420
    reference: chr 5
allele count: 1
allele frequency: 8.333333333333334e-6
allele num: 120000
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.356T>C
  hgvsp: ENSP00000424387.1:p.Ile119Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.44T>C
  hgvsp: ENSP00000438469.1:p.Ile15Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.356T>C
  hgvsp: ENSP00000422130.1:p.Ile119Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.351T>C
  hgvsp: ENST00000505012.1:c.351T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.455T>C
  hgvsp: ENSP00000387710.2:p.Ile152Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.356T>C
  hgvsp: ENSP00000265112.3:p.Ile119Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1667T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*313T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*309T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1667T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.165T>C
  hgvsp: ENST00000508361.1:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile152Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

5-33453421-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453421
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453421
    reference: chr 5
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.352T>C
  hgvsp: ENSP00000422291.1:p.Cys118Arg
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1666T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*310T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.45T>C
  hgvsp: ENST00000541634.1:c.45T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.357T>C
  hgvsp: ENST00000514259.1:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*314T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.166T>C
  hgvsp: ENSP00000427627.1:p.Cys56Arg
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1666T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.357T>C
  hgvsp: ENST00000265112.3:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.456T>C
  hgvsp: ENST00000455217.2:c.456T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.357T>C
  hgvsp: ENST00000502553.1:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys56Arg
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

5-33453424-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453424
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453424
    reference: chr 5
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*313T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*317T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.169T>C
  hgvsp: ENSP00000427627.1:p.Ter57GlnextTer3
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.360T>C
  hgvsp: ENST00000502553.1:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.459T>C
  hgvsp: ENST00000455217.2:c.459T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.360T>C
  hgvsp: ENST00000514259.1:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.355T>C
  hgvsp: ENSP00000422291.1:p.Ter119GlnextTer3
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.360T>C
  hgvsp: ENST00000265112.3:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1663T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1663T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.48T>C
  hgvsp: ENST00000541634.1:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter57GlnextTer3
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

5-33453425-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453425
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453425
    reference: chr 5
allele count: 1
allele frequency: 8.317253310266817e-6
allele num: 120232
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.460A>G
  hgvsp: ENSP00000387710.2:p.Lys154Glu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.170A>G
  hgvsp: ENST00000508361.1:c.170A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.361A>G
  hgvsp: ENSP00000424387.1:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.361A>G
  hgvsp: ENSP00000265112.3:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.356A>G
  hgvsp: ENST00000505012.1:c.356A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.361A>G
  hgvsp: ENSP00000422130.1:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1662A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*318A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.49A>G
  hgvsp: ENSP00000438469.1:p.Lys17Glu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1662A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*314A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys154Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

5-33453441-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453441
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453441
    reference: chr 5
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.377T>G
  hgvsp: ENSP00000265112.3:p.Val126Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.65T>G
  hgvsp: ENSP00000438469.1:p.Val22Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.377T>G
  hgvsp: ENSP00000424387.1:p.Val126Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1646T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.377T>G
  hgvsp: ENSP00000422130.1:p.Val126Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*15T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.476T>G
  hgvsp: ENSP00000387710.2:p.Val159Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*330T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*334T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*15T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1646T>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val159Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

5-33453445-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453445
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453445
    reference: chr 5
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.480G>A
  hgvsp: ENSP00000387710.2:p.Trp160Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.381G>A
  hgvsp: ENSP00000424387.1:p.Trp127Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1642G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.69G>A
  hgvsp: ENSP00000438469.1:p.Trp23Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*338G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*334G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.381G>A
  hgvsp: ENSP00000265112.3:p.Trp127Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422130
  ensembl transcript: ENST00000514259
  gene symbol: TARS
  hgvsc: ENST00000514259.1:c.381G>A
  hgvsp: ENSP00000422130.1:p.Trp127Ter
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1642G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp160Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD

5-33453456-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453456
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453456
    reference: chr 5
allele count: 16
allele frequency: 1.322510786728604e-4
allele num: 120982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*345G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.392G>A
  hgvsp: ENSP00000265112.3:p.Arg131His
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.392G>A
  hgvsp: ENSP00000424387.1:p.Arg131His
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*30G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1631G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.80G>A
  hgvsp: ENSP00000438469.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*30G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*349G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1631G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.491G>A
  hgvsp: ENSP00000387710.2:p.Arg164His
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg164His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

5-33453458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453458
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453458
    reference: chr 5
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.493C>T
  hgvsp: ENSP00000387710.2:p.Pro165Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1629C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*351C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*347C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.394C>T
  hgvsp: ENSP00000424387.1:p.Pro132Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*32C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*32C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1629C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.394C>T
  hgvsp: ENSP00000265112.3:p.Pro132Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.82C>T
  hgvsp: ENSP00000438469.1:p.Pro28Ser
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13048
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro165Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

5-33453459-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453459
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453459
    reference: chr 5
allele count: 1
allele frequency: 8.262823902696986e-6
allele num: 121024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*352C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1628C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.395C>T
  hgvsp: ENSP00000265112.3:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.494C>T
  hgvsp: ENSP00000387710.2:p.Pro165Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.83C>T
  hgvsp: ENSP00000438469.1:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.395C>T
  hgvsp: ENSP00000424387.1:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1628C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*348C>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro165Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

5-33453471-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453471
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453471
    reference: chr 5
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.407A>T
  hgvsp: ENSP00000265112.3:p.Asp136Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000425524
  ensembl transcript: ENST00000513066
  gene symbol: TARS
  hgvsc: ENST00000513066.1:c.*364A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.407A>T
  hgvsp: ENSP00000424387.1:p.Asp136Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1616A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1616A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*360A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*45A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.95A>T
  hgvsp: ENSP00000438469.1:p.Asp32Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.506A>T
  hgvsp: ENSP00000387710.2:p.Asp169Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*45A>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp169Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

5-33453476-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453476
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453476
    reference: chr 5
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.412A>G
  hgvsp: ENSP00000424387.1:p.Thr138Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1611A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.412A>G
  hgvsp: ENSP00000265112.3:p.Thr138Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*365A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.511A>G
  hgvsp: ENSP00000387710.2:p.Thr171Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.100A>G
  hgvsp: ENSP00000438469.1:p.Thr34Ala
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1611A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr171Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

5-33453496-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453496
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453496
    reference: chr 5
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*70T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.432T>C
  hgvsp: ENST00000502553.1:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.531T>C
  hgvsp: ENST00000455217.2:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*70T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1591T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.432T>C
  hgvsp: ENST00000265112.3:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1591T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.120T>C
  hgvsp: ENST00000541634.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*385T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23088
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5228
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe177Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

5-33453506-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453506
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453506
    reference: chr 5
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.130G>A
  hgvsp: ENSP00000438469.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1581G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*80G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.442G>A
  hgvsp: ENSP00000265112.3:p.Glu148Lys
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.442G>A
  hgvsp: ENSP00000424387.1:p.Glu148Lys
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.541G>A
  hgvsp: ENSP00000387710.2:p.Glu181Lys
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1581G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*395G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*80G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23085
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu181Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-33453507-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453507
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453507
    reference: chr 5
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.443A>T
  hgvsp: ENSP00000424387.1:p.Glu148Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.443A>T
  hgvsp: ENSP00000265112.3:p.Glu148Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.542A>T
  hgvsp: ENSP00000387710.2:p.Glu181Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*396A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*81A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1580A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*81A>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.131A>T
  hgvsp: ENSP00000438469.1:p.Glu44Val
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1580A>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu181Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

5-33453515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453515
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453515
    reference: chr 5
allele count: 2
allele frequency: 1.650682557237418e-5
allele num: 121162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*89G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.451G>A
  hgvsp: ENSP00000424387.1:p.Ala151Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.139G>A
  hgvsp: ENSP00000438469.1:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.451G>A
  hgvsp: ENSP00000265112.3:p.Ala151Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*89G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1572G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*404G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.550G>A
  hgvsp: ENSP00000387710.2:p.Ala184Thr
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1572G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2281
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala184Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

5-33453515-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453515
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453515
    reference: chr 5
allele count: 2
allele frequency: 1.650682557237418e-5
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1572G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*89G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.451G>T
  hgvsp: ENSP00000424387.1:p.Ala151Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*89G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.451G>T
  hgvsp: ENSP00000265112.3:p.Ala151Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.139G>T
  hgvsp: ENSP00000438469.1:p.Ala47Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.550G>T
  hgvsp: ENSP00000387710.2:p.Ala184Ser
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*404G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1572G>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala184Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

5-33453530-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453530
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453530
    reference: chr 5
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1557T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+13T>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1557T>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

5-33453530-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453530
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453530
    reference: chr 5
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+13T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+13T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+13T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+13T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+13T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1557T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+13T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1557T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+13T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13430
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

5-33453534-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453534
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453534
    reference: chr 5
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1553T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+17T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+17T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+17T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+17T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+17T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+17T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1553T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+17T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

5-33453535-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453535
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453535
    reference: chr 5
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1552A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+18A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1552A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22802
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/5-33453543-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453543
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453543
    reference: chr 5
allele count: 10
allele frequency: 8.255865792645674e-5
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1544A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+26A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+26A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1544A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+26A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+26A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+26A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+26A>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+26A>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

5-33453555-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453555
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453555
    reference: chr 5
allele count: 2
allele frequency: 1.651636772041093e-5
allele num: 121092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1532C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+38C>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1532C>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-33453556-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453556
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453556
    reference: chr 5
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1531A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1531A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+39A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+39A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

5-33453566-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33453566
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33453566
    reference: chr 5
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*91+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.453+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*91+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-1521T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.141+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*406+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.552+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.453+49T>C
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-1521T>C
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5221
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3581
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

5-33455000-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455000
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455000
    reference: chr 5
allele count: 2
allele frequency: 1.659613310098747e-5
allele num: 120510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-50C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-50C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-87C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-50C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-50C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-50C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-50C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-87C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-50C>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

5-33455003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455003
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455003
    reference: chr 5
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-84C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-47C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-84C>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30679
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-33455008-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455008
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455008
    reference: chr 5
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-79A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-42A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-79A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

5-33455023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455023
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455023
    reference: chr 5
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-27C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-64C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-64C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-27C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-27C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-27C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-27C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-27C>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-27C>T
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

5-33455025-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455025
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455025
    reference: chr 5
allele count: 2
allele frequency: 1.654779831543413e-5
allele num: 120862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-25A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-25A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-25A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-62A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-25A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-62A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-25A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-25A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-25A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26390
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-33455028-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455028
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455028
    reference: chr 5
allele count: 3
allele frequency: 2.481061232591221e-5
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-22C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-22C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-22C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-59C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-59C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-22C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-22C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-22C>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-22C>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

5-33455034-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455034
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455034
    reference: chr 5
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-53T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-16T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-53T>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

5-33455039-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455039
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455039
    reference: chr 5
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-11T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-11T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-48T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-11T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-48T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-11T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-11T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-11T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-11T>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

5-33455043-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455043
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455043
    reference: chr 5
allele count: 5
allele frequency: 4.128614602084125e-5
allele num: 121106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142-7T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92-7T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553-7T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92-7T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-44T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454-7T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454-7T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-44T>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407-7T>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
hgvs: c.553-7T>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

5-33455050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455050
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455050
    reference: chr 5
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-37G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142G>A
  hgvsp: ENSP00000438469.1:p.Val48Met
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553G>A
  hgvsp: ENSP00000387710.2:p.Val185Met
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454G>A
  hgvsp: ENSP00000265112.3:p.Val152Met
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454G>A
  hgvsp: ENSP00000424387.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-37G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8947
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val185Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

5-33455050-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455050
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455050
    reference: chr 5
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-37G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-37G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*407G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.142G>T
  hgvsp: ENSP00000438469.1:p.Val48Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.454G>T
  hgvsp: ENSP00000424387.1:p.Val152Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.454G>T
  hgvsp: ENSP00000265112.3:p.Val152Leu
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*92G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*92G>T
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.553G>T
  hgvsp: ENSP00000387710.2:p.Val185Leu
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val185Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

5-33455052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455052
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455052
    reference: chr 5
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*409G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.144G>A
  hgvsp: ENST00000541634.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.555G>A
  hgvsp: ENST00000455217.2:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.456G>A
  hgvsp: ENST00000502553.1:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*94G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*94G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-35G>A
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.456G>A
  hgvsp: ENST00000265112.3:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-35G>A
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34759
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.555G>A
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

5-33455065-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33455065
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 33455065
    reference: chr 5
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000438469
  ensembl transcript: ENST00000541634
  gene symbol: TARS
  hgvsc: ENST00000541634.1:c.157A>G
  hgvsp: ENSP00000438469.1:p.Ser53Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000424387
  ensembl transcript: ENST00000502553
  gene symbol: TARS
  hgvsc: ENST00000502553.1:c.469A>G
  hgvsp: ENSP00000424387.1:p.Ser157Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000422291
  ensembl transcript: ENST00000505012
  gene symbol: TARS
  hgvsc: ENST00000505012.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000420893
  ensembl transcript: ENST00000507716
  gene symbol: TARS
  hgvsc: ENST00000507716.1:c.330-22A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000265112
  ensembl transcript: ENST00000265112
  gene symbol: TARS
  hgvsc: ENST00000265112.3:c.469A>G
  hgvsp: ENSP00000265112.3:p.Ser157Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427627
  ensembl transcript: ENST00000508361
  gene symbol: TARS
  hgvsc: ENST00000508361.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000387710
  ensembl transcript: ENST00000455217
  gene symbol: TARS
  hgvsc: ENST00000455217.2:c.568A>G
  hgvsp: ENSP00000387710.2:p.Ser190Gly
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000394291
  ensembl transcript: ENST00000414361
  gene symbol: TARS
  hgvsc: ENST00000414361.2:c.128-22A>G
  variant of: http://identifiers.org/hgnc/11572
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000113407
  ensembl protein: ENSP00000427304
  ensembl transcript: ENST00000509731
  gene symbol: TARS
  hgvsc: ENST00000509731.1:c.*422A>G
  variant of: http://identifiers.org/hgnc/11572
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser190Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
reference allele: A

GenotypeQuality
all individuals: 1344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2811
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 671
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5047
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.175331738090059e-5
allele num: 45970
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.539e-1

MQ
type: SiteQuality
SIO_000300: 6.051e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

DP
type: SiteQuality
SIO_000300: 1.053874e6

GenotypeQuality
all individuals: 4397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1831
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 558
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10572
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3439
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4800
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.317870321560359e-4
allele num: 7588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.876633200385091e-5
allele num: 14542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

VQSLOD
type: SiteQuality
SIO_000300: 8.85e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

DP
type: SiteQuality
SIO_000300: 1.065491e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

QD
type: SiteQuality
SIO_000300: 1.551e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

GenotypeQuality
all individuals: 1425
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2572
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10589
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4548
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.408450704225352e-3
allele num: 710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.158894645941278e-5
allele num: 46320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5982
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.244e1

DP
type: SiteQuality
SIO_000300: 1.077509e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 1212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3350
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3948
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2583
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5243
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10654
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16171
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.81663258350375e-5
allele num: 14670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.622e1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.52e-1

DP
type: SiteQuality
SIO_000300: 1.136984e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.195e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.784e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

GenotypeQuality
all individuals: 2735
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9895
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4270
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4424
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16983
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 3645
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1880
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 3.347840642785404e-4
allele num: 47792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.753e1

VQSLOD
type: SiteQuality
SIO_000300: -5.623e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

DP
type: SiteQuality
SIO_000300: 1.21601e6

QD
type: SiteQuality
SIO_000300: 1.33e1

GenotypeQuality
all individuals: 15474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9274
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2841
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2270
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3553
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2868
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46892
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.028394714647174e-5
allele num: 14228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQ
type: SiteQuality
SIO_000300: 5.177e1

MQRankSum
type: SiteQuality
SIO_000300: -7.14e-1

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.044e0

VQSLOD
type: SiteQuality
SIO_000300: -1.444e0

DP
type: SiteQuality
SIO_000300: 1.250541e6

GenotypeQuality
all individuals: 3214
bin: 3.75e1
variant carriers: 23

GenotypeQuality
all individuals: 1800
bin: 1.25e1
variant carriers: 137

GenotypeQuality
all individuals: 3621
bin: 2.5e0
variant carriers: 251

GenotypeQuality
all individuals: 1960
bin: 1.75e1
variant carriers: 77

GenotypeQuality
all individuals: 1424
bin: 5.75e1
variant carriers: 24

GenotypeQuality
all individuals: 666
bin: 9.25e1
variant carriers: 34

GenotypeQuality
all individuals: 3099
bin: 7.5e0
variant carriers: 192

GenotypeQuality
all individuals: 3584
bin: 2.75e1
variant carriers: 40

GenotypeQuality
all individuals: 1129
bin: 8.25e1
variant carriers: 24

GenotypeQuality
all individuals: 2030
bin: 4.25e1
variant carriers: 15

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 18

GenotypeQuality
all individuals: 4145
bin: 3.25e1
variant carriers: 27

GenotypeQuality
all individuals: 3757
bin: 9.75e1
variant carriers: 946

GenotypeQuality
all individuals: 7851
bin: 2.25e1
variant carriers: 51

GenotypeQuality
all individuals: 3199
bin: 6.75e1
variant carriers: 25

GenotypeQuality
all individuals: 10950
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 1621
bin: 5.25e1
variant carriers: 23

GenotypeQuality
all individuals: 1854
bin: 4.75e1
variant carriers: 38

GenotypeQuality
all individuals: 1373
bin: 7.25e1
variant carriers: 42

GenotypeQuality
all individuals: 1515
bin: 7.75e1
variant carriers: 30

European (Non-Finnish)
type: Population
allele count: 351
allele frequency: 7.88445123320904e-3
allele num: 44518
num of homozygotes: 16

African
type: Population
allele count: 30
allele frequency: 4.225352112676056e-3
allele num: 7100
num of homozygotes: 3

Other
type: Population
allele count: 8
allele frequency: 1.162790697674419e-2
allele num: 688
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 38
allele frequency: 6.613296206056387e-3
allele num: 5746
num of homozygotes: 1

South Asian
type: Population
allele count: 441
allele frequency: 3.297442799461642e-2
allele num: 13374
num of homozygotes: 55

Latino
type: Population
allele count: 345
allele frequency: 4.732510288065844e-2
allele num: 7290
num of homozygotes: 78

East Asian
type: Population
allele count: 208
allele frequency: 3.874813710879284e-2
allele num: 5368
num of homozygotes: 40

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 1.244335e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.354e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 4145
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3214
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1800
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1515
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3199
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3621
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1960
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7851
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 527
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3757
bin: 9.75e1
variant carriers: 513

GenotypeQuality
all individuals: 1373
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1424
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3099
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2030
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10950
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1854
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1129
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3584
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 666
bin: 9.25e1
variant carriers: 1

South Asian
type: Population
allele count: 8
allele frequency: 5.98175564528189e-4
allele num: 13374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 86
allele frequency: 1.496693351896972e-2
allele num: 5746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 414
allele frequency: 9.299609146861943e-3
allele num: 44518
num of homozygotes: 4

Other
type: Population
allele count: 3
allele frequency: 4.36046511627907e-3
allele num: 688
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 2.253521126760564e-3
allele num: 7100
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.743484224965707e-4
allele num: 7290
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.244335e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 31

GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 238

GenotypeQuality
all individuals: 2497
bin: 7.5e0
variant carriers: 495

GenotypeQuality
all individuals: 605
bin: 6.75e1
variant carriers: 128

GenotypeQuality
all individuals: 1224
bin: 3.25e1
variant carriers: 464

GenotypeQuality
all individuals: 384
bin: 8.25e1
variant carriers: 55

GenotypeQuality
all individuals: 1960
bin: 2.25e1
variant carriers: 610

GenotypeQuality
all individuals: 935
bin: 4.25e1
variant carriers: 460

GenotypeQuality
all individuals: 1237
bin: 3.75e1
variant carriers: 594

GenotypeQuality
all individuals: 1164
bin: 2.75e1
variant carriers: 387

GenotypeQuality
all individuals: 33138
bin: 2.5e0
variant carriers: 576

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 29

GenotypeQuality
all individuals: 873
bin: 4.75e1
variant carriers: 415

GenotypeQuality
all individuals: 1069
bin: 9.75e1
variant carriers: 124

GenotypeQuality
all individuals: 1567
bin: 1.25e1
variant carriers: 523

GenotypeQuality
all individuals: 799
bin: 6.25e1
variant carriers: 175

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 70

GenotypeQuality
all individuals: 1446
bin: 1.75e1
variant carriers: 543

GenotypeQuality
all individuals: 815
bin: 5.25e1
variant carriers: 345

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 87

Latino
type: Population
allele count: 87
allele frequency: 8.285714285714285e-2
allele num: 1050
num of homozygotes: 0

Other
type: Population
allele count: 38
allele frequency: 1.919191919191919e-1
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 286
allele frequency: 9.364767518009168e-2
allele num: 3054
num of homozygotes: 1

East Asian
type: Population
allele count: 78
allele frequency: 8.609271523178808e-2
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 201
allele frequency: 1.237684729064039e-1
allele num: 1624
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 402
allele frequency: 2.199124726477024e-1
allele num: 1828
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1452
allele frequency: 1.381278538812785e-1
allele num: 10512
num of homozygotes: 3

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.243e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.69e1

DP
type: SiteQuality
SIO_000300: 1.317106e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 3.49e0

South Asian
type: Population
allele count: 437
allele frequency: 1.430910281597904e-1
allele num: 3054
num of homozygotes: 0

Other
type: Population
allele count: 29
allele frequency: 1.464646464646465e-1
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1594
allele frequency: 1.516362252663623e-1
allele num: 10512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

DP
type: SiteQuality
SIO_000300: 1.317106e6

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.69e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.243e-1

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 64

GenotypeQuality
all individuals: 1960
bin: 2.25e1
variant carriers: 85

GenotypeQuality
all individuals: 1224
bin: 3.25e1
variant carriers: 48

GenotypeQuality
all individuals: 1567
bin: 1.25e1
variant carriers: 88

GenotypeQuality
all individuals: 384
bin: 8.25e1
variant carriers: 89

GenotypeQuality
all individuals: 33138
bin: 2.5e0
variant carriers: 138

GenotypeQuality
all individuals: 1164
bin: 2.75e1
variant carriers: 55

GenotypeQuality
all individuals: 1237
bin: 3.75e1
variant carriers: 64

GenotypeQuality
all individuals: 605
bin: 6.75e1
variant carriers: 78

GenotypeQuality
all individuals: 873
bin: 4.75e1
variant carriers: 70

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 74

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 68

GenotypeQuality
all individuals: 935
bin: 4.25e1
variant carriers: 59

GenotypeQuality
all individuals: 2497
bin: 7.5e0
variant carriers: 94

GenotypeQuality
all individuals: 1446
bin: 1.75e1
variant carriers: 80

GenotypeQuality
all individuals: 1069
bin: 9.75e1
variant carriers: 401

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 76

GenotypeQuality
all individuals: 815
bin: 5.25e1
variant carriers: 62

GenotypeQuality
all individuals: 799
bin: 6.25e1
variant carriers: 46

GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 73

Latino
type: Population
allele count: 56
allele frequency: 5.333333333333334e-2
allele num: 1050
num of homozygotes: 0

South Asian
type: Population
allele count: 262
allele frequency: 8.578912901113293e-2
allele num: 3054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 666
allele frequency: 6.335616438356165e-2
allele num: 10512
num of homozygotes: 0

African
type: Population
allele count: 90
allele frequency: 5.541871921182266e-2
allele num: 1624
num of homozygotes: 0

East Asian
type: Population
allele count: 43
allele frequency: 4.746136865342163e-2
allele num: 906
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 5.555555555555555e-2
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 124
allele frequency: 6.783369803063458e-2
allele num: 1828
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.49e0

DP
type: SiteQuality
SIO_000300: 1.317106e6

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQ
type: SiteQuality
SIO_000300: 5.69e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.243e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

GenotypeQuality
all individuals: 935
bin: 4.25e1
variant carriers: 42

GenotypeQuality
all individuals: 1164
bin: 2.75e1
variant carriers: 97

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1446
bin: 1.75e1
variant carriers: 126

GenotypeQuality
all individuals: 384
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1237
bin: 3.75e1
variant carriers: 107

GenotypeQuality
all individuals: 2497
bin: 7.5e0
variant carriers: 175

GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 32

GenotypeQuality
all individuals: 605
bin: 6.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1960
bin: 2.25e1
variant carriers: 86

GenotypeQuality
all individuals: 33138
bin: 2.5e0
variant carriers: 162

GenotypeQuality
all individuals: 815
bin: 5.25e1
variant carriers: 39

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 873
bin: 4.75e1
variant carriers: 33

GenotypeQuality
all individuals: 1069
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1567
bin: 1.25e1
variant carriers: 118

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 799
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1224
bin: 3.25e1
variant carriers: 97

East Asian
type: Population
allele count: 7
allele frequency: 7.72626931567329e-3
allele num: 906
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.515151515151515e-2
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 28
allele frequency: 1.724137931034483e-2
allele num: 1624
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.80952380952381e-3
allele num: 1050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 163
allele frequency: 1.550608828006088e-2
allele num: 10512
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 7.858546168958742e-3
allele num: 3054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 32
allele frequency: 1.75054704595186e-2
allele num: 1828
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.317106e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.243e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.69e1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 3.49e0

GenotypeQuality
all individuals: 33138
bin: 2.5e0
variant carriers: 18

GenotypeQuality
all individuals: 1237
bin: 3.75e1
variant carriers: 25

GenotypeQuality
all individuals: 935
bin: 4.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1446
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1224
bin: 3.25e1
variant carriers: 13

GenotypeQuality
all individuals: 2497
bin: 7.5e0
variant carriers: 33

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 815
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1164
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1567
bin: 1.25e1
variant carriers: 19

GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1069
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1960
bin: 2.25e1
variant carriers: 16

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 799
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 605
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 4.75e1
variant carriers: 17

East Asian
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 2.463054187192118e-3
allele num: 1624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 2.735229759299781e-3
allele num: 1828
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 1.964636542239686e-3
allele num: 3054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 3.0441400304414e-3
allele num: 10512
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.523809523809524e-4
allele num: 1050
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.050505050505051e-3
allele num: 198
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.49e0

MQ
type: SiteQuality
SIO_000300: 5.69e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.243e-1

DP
type: SiteQuality
SIO_000300: 1.317106e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

African
type: Population
allele count: 18
allele frequency: 1.108374384236453e-2
allele num: 1624
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.333333333333333e-2
allele num: 1050
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 1.01010101010101e-2
allele num: 198
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.243e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 3.49e0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQ
type: SiteQuality
SIO_000300: 5.69e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 1.317106e6

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 758
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 31659
bin: 2.5e0
variant carriers: 209

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 747
bin: 2.25e1
variant carriers: 39

GenotypeQuality
all individuals: 659
bin: 1.25e1
variant carriers: 130

GenotypeQuality
all individuals: 457
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 724
bin: 1.75e1
variant carriers: 59

GenotypeQuality
all individuals: 1612
bin: 7.5e0
variant carriers: 157

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 697
bin: 2.75e1
variant carriers: 27

GenotypeQuality
all individuals: 327
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 84
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 219
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 52
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 477
bin: 4.25e1
variant carriers: 9

GenotypeQuality
all individuals: 131
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 361
bin: 9.75e1
variant carriers: 221

GenotypeQuality
all individuals: 788
bin: 3.25e1
variant carriers: 16

European (Finnish)
type: Population
allele count: 9
allele frequency: 2.093023255813953e-2
allele num: 430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 91
allele frequency: 3.599683544303797e-2
allele num: 2528
num of homozygotes: 0

South Asian
type: Population
allele count: 56
allele frequency: 2.659069325735992e-2
allele num: 2106
num of homozygotes: 3

East Asian
type: Population
allele count: 51
allele frequency: 3.455284552845529e-2
allele num: 1476
num of homozygotes: 7

African
type: Population
allele count: 39
allele frequency: 4.974489795918367e-2
allele num: 784
num of homozygotes: 2

Other
type: Population
allele count: 3
allele frequency: 4.545454545454546e-2
allele num: 66
num of homozygotes: 0

Latino
type: Population
allele count: 65
allele frequency: 2.946509519492294e-2
allele num: 2206
num of homozygotes: 7

QD
type: SiteQuality
SIO_000300: 7.24e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 1.119361e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.544e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

GenotypeQuality
all individuals: 189
bin: 2.25e1
variant carriers: 18

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 15

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

GenotypeQuality
all individuals: 26
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 38530
bin: 2.5e0
variant carriers: 16

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2736
bin: 7.5e0
variant carriers: 25

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 12

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 9

GenotypeQuality
all individuals: 25
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 312
bin: 1.25e1
variant carriers: 16

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 39
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 12

GenotypeQuality
all individuals: 36
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 25
bin: 7.25e1
variant carriers: 2

East Asian
type: Population
allele count: 11
allele frequency: 8.461538461538462e-2
allele num: 130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 30
allele frequency: 4.322766570605188e-2
allele num: 694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 6.172839506172839e-2
allele num: 162
num of homozygotes: 1

Latino
type: Population
allele count: 12
allele frequency: 6.060606060606061e-2
allele num: 198
num of homozygotes: 0

African
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allele count: 13
allele frequency: 6.372549019607843e-2
allele num: 204
num of homozygotes: 0

South Asian
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allele count: 9
allele frequency: 2.662721893491124e-2
allele num: 338
num of homozygotes: 1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.955e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

BaseQRankSum
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SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

QD
type: SiteQuality
SIO_000300: 2.65e0

DP
type: SiteQuality
SIO_000300: 1.352981e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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allele count: 3
allele frequency: 7.575757575757576e-3
allele num: 396
num of homozygotes: 0

African
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allele count: 5
allele frequency: 1.033057851239669e-2
allele num: 484
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.639344262295082e-2
allele num: 244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 2.777777777777778e-2
allele num: 252
num of homozygotes: 0

South Asian
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allele count: 5
allele frequency: 9.541984732824428e-3
allele num: 524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 6.97292863002461e-3
allele num: 2438
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.179e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.856e1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 7.4e-1

DP
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SIO_000300: 1.532624e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.439024390243902e-3
allele num: 410
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.590673575129534e-3
allele num: 1158
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.491488193300384e-4
allele num: 7284
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 4.464285714285714e-3
allele num: 448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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DP
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SIO_000300: 1.63719e6

FS
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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SIO_000300: 1.39e0

MQ
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 824
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 frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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ReadPosRankSum
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SIO_000300: 8.37e-1

BaseQRankSum
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SIO_000300: -1.614e0

DP
type: SiteQuality
SIO_000300: 1.76486e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: -5.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 3.69e0

GenotypeDepth
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.094091903719913e-4
allele num: 9140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16010
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62462
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

DP
type: SiteQuality
SIO_000300: 1.76486e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.614e0

ClippingRankSum
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SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 3.69e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.201946783644456e-5
allele num: 62462
num of homozygotes: 0

South Asian
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allele num: 16010
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

ClippingRankSum
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SIO_000300: 6.5e-2

FS
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

DP
type: SiteQuality
SIO_000300: 1.76486e6

MQ
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele num: 57194
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

East Asian
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Latino
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African
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European (Non-Finnish)
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South Asian
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Other
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Other
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African
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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DP
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MQ
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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South Asian
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ReadPosRankSum
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DP
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ClippingRankSum
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MQRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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South Asian
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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Other
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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FS
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QD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6510
num of homozygotes: 0

East Asian
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African
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Latino
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South Asian
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Other
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European (Non-Finnish)
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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African
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South Asian
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520218911523259e-5
allele num: 65780
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.528e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
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SIO_000300: 1.988601e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.002e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.191e0

FS
type: SiteQuality
SIO_000300: 1.657e0

MQ
type: SiteQuality
SIO_000300: 5.795e1

MQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

GenotypeDepth
all individuals: 12993
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 12891
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variant carriers: 3

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 6095
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variant carriers: 204

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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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 13342
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 187
allele frequency: 1.842364532019704e-2
allele num: 10150
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.215657670799903e-4
allele num: 65808
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

Latino
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allele count: 12
allele frequency: 1.046937707206421e-3
allele num: 11462
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.48e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.325e1

BaseQRankSum
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SIO_000300: 3.97e0

InbreedingCoeff
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SIO_000300: 2.1e-3

ClippingRankSum
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SIO_000300: -3.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

DP
type: SiteQuality
SIO_000300: 1.999848e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2272
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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
all individuals: 13363
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variant carriers: 0

GenotypeQuality
all individuals: 22600
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516300227445034e-5
allele num: 65950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.897e1

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.231e-1

QD
type: SiteQuality
SIO_000300: 1.564e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.476e0

DP
type: SiteQuality
SIO_000300: 1.994436e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.49e0

GenotypeDepth
all individuals: 629
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 3559
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 5206
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variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.326e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e0

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 1.99489e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e0

VQSLOD
type: SiteQuality
SIO_000300: -2.964e0

QD
type: SiteQuality
SIO_000300: 2.187e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 6158
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variant carriers: 1

GenotypeQuality
all individuals: 3559
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.813542688910697e-5
allele num: 10190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8478
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: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66088
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

FS
type: SiteQuality
SIO_000300: 3.388e0

MQRankSum
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SIO_000300: -1.256e0

VQSLOD
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QD
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BaseQRankSum
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SIO_000300: 3.85e0

ClippingRankSum
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SIO_000300: -1.007e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.898e1

DP
type: SiteQuality
SIO_000300: 1.996388e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66122
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179245283018868e-4
allele num: 8480
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

DP
type: SiteQuality
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BaseQRankSum
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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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ReadPosRankSum
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SIO_000300: -4.1e-1

MQRankSum
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SIO_000300: 8.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
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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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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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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 6176
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

Latino
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African
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allele num: 10300
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Other
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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QD
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

African
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Other
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South Asian
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allele frequency: 7.27802037845706e-4
allele num: 16488
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 2.600104004160167e-4
allele num: 11538
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East Asian
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

African
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.935e1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

East Asian
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Other
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: -4.37e-1

MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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FS
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SIO_000300: 0.0e0

QD
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11550
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 3.03030303030303e-4
allele num: 6600
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66622
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Other
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InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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African
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Other
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QD
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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South Asian
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FS
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MQRankSum
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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DP
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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SIO_000300: 4.943e0

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.647e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 11558
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8612
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.001831116981359e-5
allele num: 66626
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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QD
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MQRankSum
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ClippingRankSum
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FS
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele frequency: 8.652015919709292e-5
allele num: 11558
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: 6606
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

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

East Asian
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allele count: 0
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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MQ
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DP
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ClippingRankSum
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SIO_000300: -3.67e-1

ReadPosRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

African
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

DP
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FS
type: SiteQuality
SIO_000300: 7.05e-1

MQRankSum
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QD
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InbreedingCoeff
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MQ
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SIO_000300: 5.909e1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002642325246217e-5
allele num: 66608
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.909e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 6.06134076857801e-5
allele num: 16498
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African
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East Asian
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Other
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Finnish)
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African
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Latino
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East Asian
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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DP
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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FS
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DP
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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Other
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East Asian
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Latino
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African
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allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -8.31e-1

DP
type: SiteQuality
SIO_000300: 2.000972e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

MQ
type: SiteQuality
SIO_000300: 5.888e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.629e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.317e0

FS
type: SiteQuality
SIO_000300: 3.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.39e-1

DP
type: SiteQuality
SIO_000300: 2.000738e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.558e0

MQ
type: SiteQuality
SIO_000300: 5.856e1

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
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
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

MQ
type: SiteQuality
SIO_000300: 5.85e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 8.781000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.604e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 2.00132e6

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: 2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.960015680125441e-4
allele num: 10204
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: 8644
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.52e-1

FS
type: SiteQuality
SIO_000300: 5.769e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 9.93e0

DP
type: SiteQuality
SIO_000300: 1.829149e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.185056902523504e-5
allele num: 16168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 4.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.651e-1

DP
type: SiteQuality
SIO_000300: 1.830252e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.898e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.063e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.848559e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

African
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South Asian
type: Population
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allele frequency: 0.0e0
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East Asian
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

South Asian
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allele count: 2
allele frequency: 1.222493887530562e-4
allele num: 16360
num of homozygotes: 0

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

African
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Latino
type: Population
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East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

Other
type: Population
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allele num: 900
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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MQ
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InbreedingCoeff
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.286e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.856242e6

VQSLOD
type: SiteQuality
SIO_000300: -2.961e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.857781e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.294e0

QD
type: SiteQuality
SIO_000300: 1.449e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: -5.51e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.779010633379565e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

QD
type: SiteQuality
SIO_000300: 1.329e1

MQRankSum
type: SiteQuality
SIO_000300: 8.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.859105e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.422e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.749e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.98e-1

FS
type: SiteQuality
SIO_000300: 3.519e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e0

DP
type: SiteQuality
SIO_000300: 1.861031e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
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

DP
type: SiteQuality
SIO_000300: 1.861031e6

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.519e0

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -9.98e-1

VQSLOD
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
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SIO_000300: 1.422e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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BaseQRankSum
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DP
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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