14-100813073-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813073
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813073
    reference: chr 14
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.703+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.84+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7055G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.826+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.838+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.826+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.703+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.703+10C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.826+10C>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12647
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-100813073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813073
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813073
    reference: chr 14
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7055G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.703+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.703+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.826+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.826+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.838+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.826+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.703+10C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.84+10C>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12647
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-100813075-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813075
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813075
    reference: chr 14
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.703+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.826+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7053C>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.84+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.826+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.703+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.703+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.826+8G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.838+8G>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 7.25e1
  variant carriers: 0
hgvs: c.826+8G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-100813077-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813077
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813077
    reference: chr 14
allele count: 91123
allele frequency: 7.513192177039015e-1
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.703+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.84+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.703+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.703+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.826+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.838+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.826+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.826+6A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7051T>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 7.75e1
  variant carriers: 2197
genotype depth: GenotypeDepth
  all individuals: 6601
  bin: 4.75e1
  variant carriers: 6471
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 4.25e1
  variant carriers: 5356
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.25e1
  variant carriers: 561
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.75e1
  variant carriers: 1219
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 6.75e1
  variant carriers: 4293
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 6305
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.75e1
  variant carriers: 1251
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.25e1
  variant carriers: 5292
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 9.25e1
  variant carriers: 911
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 3.75e1
  variant carriers: 3930
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 3.25e1
  variant carriers: 2417
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 9.75e1
  variant carriers: 4358
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 5.25e1
  variant carriers: 6671
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 8.25e1
  variant carriers: 1682
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 7.25e1
  variant carriers: 3230
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 272
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 8.25e1
  variant carriers: 406
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 15
hgvs: c.826+6A>G
num of homozygotes: 34758
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/14-100813084-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813084
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813084
    reference: chr 14
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.837T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.702T>G
  hgvsp: ENSP00000351481.4:p.Ile234Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.702T>G
  hgvsp: ENSP00000451887.1:p.Ile234Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7044A>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.825T>G
  hgvsp: ENSP00000347495.2:p.Ile275Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.825T>G
  hgvsp: ENSP00000376620.2:p.Ile275Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.83T>G
  hgvsp: ENSP00000451891.1:p.Ile28Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.702T>G
  hgvsp: ENSP00000339485.5:p.Ile234Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.825T>G
  hgvsp: ENSP00000451460.1:p.Ile275Met
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile275Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

14-100813092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813092
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813092
    reference: chr 14
allele count: 13
allele frequency: 1.071281417387721e-4
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.75G>A
  hgvsp: ENSP00000451891.1:p.Asp26Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.694G>A
  hgvsp: ENSP00000351481.4:p.Asp232Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.817G>A
  hgvsp: ENSP00000451460.1:p.Asp273Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.817G>A
  hgvsp: ENSP00000376620.2:p.Asp273Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.829G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.817G>A
  hgvsp: ENSP00000347495.2:p.Asp273Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.694G>A
  hgvsp: ENSP00000451887.1:p.Asp232Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7036C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.694G>A
  hgvsp: ENSP00000339485.5:p.Asp232Asn
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp273Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

14-100813093-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813093
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813093
    reference: chr 14
allele count: 5
allele frequency: 4.120177332432388e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7035G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.816C>T
  hgvsp: ENST00000557135.1:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.74C>T
  hgvsp: ENST00000554601.1:c.74C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.828C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.693C>T
  hgvsp: ENST00000556645.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.693C>T
  hgvsp: ENST00000358655.4:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.693C>T
  hgvsp: ENST00000344102.5:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.816C>T
  hgvsp: ENST00000392882.2:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.816C>T
  hgvsp: ENST00000355338.2:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8167
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser272Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

14-100813098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813098
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813098
    reference: chr 14
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.811G>A
  hgvsp: ENSP00000451460.1:p.Asp271Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.823G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7030C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.811G>A
  hgvsp: ENSP00000376620.2:p.Asp271Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.688G>A
  hgvsp: ENSP00000339485.5:p.Asp230Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.688G>A
  hgvsp: ENSP00000451887.1:p.Asp230Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.688G>A
  hgvsp: ENSP00000351481.4:p.Asp230Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.811G>A
  hgvsp: ENSP00000347495.2:p.Asp271Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.69G>A
  hgvsp: ENSP00000451891.1:p.Asp24Asn
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp271Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

14-100813100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813100
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813100
    reference: chr 14
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.686C>T
  hgvsp: ENSP00000451887.1:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.821C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.686C>T
  hgvsp: ENSP00000339485.5:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.809C>T
  hgvsp: ENSP00000451460.1:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.809C>T
  hgvsp: ENSP00000376620.2:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7028G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.686C>T
  hgvsp: ENSP00000351481.4:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.67C>T
  hgvsp: ENSP00000451891.1:p.Thr23Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.809C>T
  hgvsp: ENSP00000347495.2:p.Thr270Ile
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2708
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3548
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr270Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

14-100813102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813102
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813102
    reference: chr 14
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.684C>T
  hgvsp: ENST00000556645.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.807C>T
  hgvsp: ENST00000557135.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.819C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.65C>T
  hgvsp: ENST00000554601.1:c.65C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.807C>T
  hgvsp: ENST00000355338.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.684C>T
  hgvsp: ENST00000358655.4:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.807C>T
  hgvsp: ENST00000392882.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.684C>T
  hgvsp: ENST00000344102.5:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7026G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6315
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe269Phe
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

14-100813108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813108
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813108
    reference: chr 14
allele count: 63
allele frequency: 5.191936839676287e-4
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.59C>T
  hgvsp: ENST00000554601.1:c.59C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.801C>T
  hgvsp: ENST00000392882.2:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.678C>T
  hgvsp: ENST00000553395.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.678C>T
  hgvsp: ENST00000344102.5:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.678C>T
  hgvsp: ENST00000556645.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.813C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7020G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.801C>T
  hgvsp: ENST00000557135.1:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.678C>T
  hgvsp: ENST00000358655.4:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.801C>T
  hgvsp: ENST00000355338.2:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14810
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25892
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe267Phe
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

14-100813126-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813126
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813126
    reference: chr 14
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.41C>A
  hgvsp: ENSP00000451891.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.795C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.660C>A
  hgvsp: ENSP00000451251.1:p.Asn220Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.660C>A
  hgvsp: ENSP00000451887.1:p.Asn220Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.783C>A
  hgvsp: ENSP00000347495.2:p.Asn261Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7002G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.783C>A
  hgvsp: ENSP00000376620.2:p.Asn261Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.660C>A
  hgvsp: ENSP00000351481.4:p.Asn220Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.660C>A
  hgvsp: ENSP00000339485.5:p.Asn220Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.660C>A
  hgvsp: ENSP00000451490.1:p.Asn220Lys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.783C>A
  hgvsp: ENSP00000451460.1:p.Asn261Lys
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn261Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-100813127-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813127
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813127
    reference: chr 14
allele count: 5
allele frequency: 4.120652711389484e-5
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-7001T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.782A>G
  hgvsp: ENSP00000451460.1:p.Asn261Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.782A>G
  hgvsp: ENSP00000347495.2:p.Asn261Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.659A>G
  hgvsp: ENSP00000351481.4:p.Asn220Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.782A>G
  hgvsp: ENSP00000376620.2:p.Asn261Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.659A>G
  hgvsp: ENSP00000451887.1:p.Asn220Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.659A>G
  hgvsp: ENSP00000451251.1:p.Asn220Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.794A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.40A>G
  hgvsp: ENSP00000451891.1:p.Asn14Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.659A>G
  hgvsp: ENSP00000451490.1:p.Asn220Ser
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.659A>G
  hgvsp: ENSP00000339485.5:p.Asn220Ser
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn261Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-100813137-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813137
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813137
    reference: chr 14
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.30G>T
  hgvsp: ENSP00000451891.1:p.Val11Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.784G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.649G>T
  hgvsp: ENSP00000339485.5:p.Val217Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.772G>T
  hgvsp: ENSP00000376620.2:p.Val258Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.649G>T
  hgvsp: ENSP00000351481.4:p.Val217Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.772G>T
  hgvsp: ENSP00000347495.2:p.Val258Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.649G>T
  hgvsp: ENSP00000451490.1:p.Val217Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.649G>T
  hgvsp: ENSP00000451251.1:p.Val217Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6991C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.649G>T
  hgvsp: ENSP00000451887.1:p.Val217Phe
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.772G>T
  hgvsp: ENSP00000451460.1:p.Val258Phe
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val258Phe
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

14-100813139-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813139
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813139
    reference: chr 14
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.782A>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6989T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.770A>T
  hgvsp: ENSP00000451460.1:p.His257Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.647A>T
  hgvsp: ENSP00000451251.1:p.His216Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.770A>T
  hgvsp: ENSP00000347495.2:p.His257Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.647A>T
  hgvsp: ENSP00000451490.1:p.His216Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.647A>T
  hgvsp: ENSP00000451887.1:p.His216Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.647A>T
  hgvsp: ENSP00000339485.5:p.His216Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.770A>T
  hgvsp: ENSP00000376620.2:p.His257Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.28A>T
  hgvsp: ENSP00000451891.1:p.His10Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.647A>T
  hgvsp: ENSP00000351481.4:p.His216Leu
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His257Leu
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

14-100813152-TCAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813152
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813149
    reference: chr 14
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.754_756delGTG
  hgvsp: ENSP00000376620.2:p.Val252del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.754_756delGTG
  hgvsp: ENSP00000347495.2:p.Val252del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.631_633delGTG
  hgvsp: ENSP00000351481.4:p.Val211del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.631_633delGTG
  hgvsp: ENSP00000451251.1:p.Val211del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.631_633delGTG
  hgvsp: ENSP00000339485.5:p.Val211del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.631_633delGTG
  hgvsp: ENSP00000451887.1:p.Val211del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.12_14delGTG
  hgvsp: ENSP00000451891.1:p.Val5del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.754_756delGTG
  hgvsp: ENSP00000451460.1:p.Val252del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.631_633delGTG
  hgvsp: ENSP00000451490.1:p.Val211del
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.766_768delGTG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6972_115-6970delCAC
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val252del
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: TCAC
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

14-100813159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813159
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813159
    reference: chr 14
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451891
  ensembl transcript: ENST00000554601
  gene symbol: WARS
  hgvsc: ENST00000554601.1:c.8T>C
  hgvsp: ENST00000554601.1:c.8T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.750T>C
  hgvsp: ENST00000355338.2:c.750T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.627T>C
  hgvsp: ENST00000556504.1:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.627T>C
  hgvsp: ENST00000553395.1:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.750T>C
  hgvsp: ENST00000557135.1:c.750T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.762T>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.627T>C
  hgvsp: ENST00000344102.5:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.627T>C
  hgvsp: ENST00000556645.1:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.750T>C
  hgvsp: ENST00000392882.2:c.750T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6969A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.627T>C
  hgvsp: ENST00000358655.4:c.627T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn250Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

14-100813175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813175
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813175
    reference: chr 14
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6953G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.734C>T
  hgvsp: ENSP00000347495.2:p.Ser245Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.611C>T
  hgvsp: ENSP00000451490.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.746C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.611C>T
  hgvsp: ENSP00000451887.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.611C>T
  hgvsp: ENSP00000451251.1:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.734C>T
  hgvsp: ENSP00000376620.2:p.Ser245Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.734C>T
  hgvsp: ENSP00000451460.1:p.Ser245Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.611C>T
  hgvsp: ENSP00000351481.4:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.611C>T
  hgvsp: ENSP00000339485.5:p.Ser204Leu
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser245Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

14-100813178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813178
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813178
    reference: chr 14
allele count: 1
allele frequency: 8.259275166011431e-6
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.608G>A
  hgvsp: ENSP00000351481.4:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.608G>A
  hgvsp: ENSP00000451251.1:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6950C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.608G>A
  hgvsp: ENSP00000451887.1:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.731G>A
  hgvsp: ENSP00000376620.2:p.Ser244Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.608G>A
  hgvsp: ENSP00000451490.1:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.731G>A
  hgvsp: ENSP00000347495.2:p.Ser244Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.743G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.608G>A
  hgvsp: ENSP00000339485.5:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.731G>A
  hgvsp: ENSP00000451460.1:p.Ser244Asn
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14663
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser244Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

14-100813196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813196
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813196
    reference: chr 14
allele count: 3
allele frequency: 2.489461280578883e-5
allele num: 120508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-13G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6932C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-13G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24709
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

14-100813197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813197
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813197
    reference: chr 14
allele count: 89
allele frequency: 7.389571570906676e-4
allele num: 120440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6931G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-14C>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7102
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14076
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24625
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 2
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/14-100813198-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813198
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813198
    reference: chr 14
allele count: 3
allele frequency: 2.491487417988539e-5
allele num: 120410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6930A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-15T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-15T>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14028
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-100813199-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813199
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813199
    reference: chr 14
allele count: 1
allele frequency: 8.308960382876895e-6
allele num: 120352
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6929G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-16C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-16C>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24402
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3269
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/14-100813214-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813214
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813214
    reference: chr 14
allele count: 5
allele frequency: 4.18872729709805e-5
allele num: 119368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6914C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-31G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-31G>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23085
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

14-100813214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813214
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813214
    reference: chr 14
allele count: 3
allele frequency: 2.51323637825883e-5
allele num: 119368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-31G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6914C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

14-100813221-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813221
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813221
    reference: chr 14
allele count: 2
allele frequency: 1.683898561950628e-5
allele num: 118772
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6907C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-38G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-38G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16222
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3827
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

14-100813222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813222
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813222
    reference: chr 14
allele count: 4
allele frequency: 3.373762250974174e-5
allele num: 118562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6906G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-39C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-39C>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11142
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

14-100813223-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813223
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813223
    reference: chr 14
allele count: 3
allele frequency: 2.532372157412253e-5
allele num: 118466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6905G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-40C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-40C>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8565
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5262
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-100813224-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813224
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813224
    reference: chr 14
allele count: 2
allele frequency: 1.687251130458257e-5
allele num: 118536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6904C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-41G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-41G>C
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

14-100813224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813224
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813224
    reference: chr 14
allele count: 881
allele frequency: 7.432341229668624e-3
allele num: 118536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-41G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6904C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 1.75e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 1.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 8348
  bin: 3.25e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 2.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 3.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 2.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 4.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4369
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4582
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6762
  bin: 9.75e1
  variant carriers: 863
num of homozygotes: 8
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-100813226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813226
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813226
    reference: chr 14
allele count: 1
allele frequency: 8.454371755634839e-6
allele num: 118282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6902T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-43A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-43A>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12206
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-100813230-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100813230
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100813230
    reference: chr 14
allele count: 2
allele frequency: 1.701664227614607e-5
allele num: 117532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.603-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.726-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.603-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.726-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.738-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-6898C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.603-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.603-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.726-47G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.603-47G>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10706
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

14-100819973-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100819973
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100819973
    reference: chr 14
allele count: 6
allele frequency: 5.064316823660488e-5
allele num: 118476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-155T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+51A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+51A>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23877
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-100819977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100819977
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100819977
    reference: chr 14
allele count: 1
allele frequency: 8.448371998715848e-6
allele num: 118366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-151C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+47G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+47G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-100819994-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100819994
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100819994
    reference: chr 14
allele count: 2
allele frequency: 1.681604923739217e-5
allele num: 118934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+30A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-134T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+30A>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9231
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

14-100820005-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820005
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820005
    reference: chr 14
allele count: 1
allele frequency: 8.348220994106157e-6
allele num: 119786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-123C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+19G>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+19G>C
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

14-100820008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820008
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820008
    reference: chr 14
allele count: 4
allele frequency: 3.327454829800686e-5
allele num: 120212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-120G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+16C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+16C>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

14-100820010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820010
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820010
    reference: chr 14
allele count: 12
allele frequency: 9.97423323082038e-5
allele num: 120310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-118C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+14G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+14G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9354
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-100820011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820011
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820011
    reference: chr 14
allele count: 25
allele frequency: 2.073828287017835e-4
allele num: 120550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+13C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-117G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

14-100820019-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820019
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820020
    reference: chr 14
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.602+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.725+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.737+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.602+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.725+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.725+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.602+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.628+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.602+4dupA
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-107dupT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.602+4dupA
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.725+4dupA
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

14-100820026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820026
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820026
    reference: chr 14
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-102C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.723G>A
  hgvsp: ENSP00000347495.2:p.Met241Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.723G>A
  hgvsp: ENSP00000376620.2:p.Met241Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.600G>A
  hgvsp: ENSP00000451490.1:p.Met200Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.600G>A
  hgvsp: ENSP00000339485.5:p.Met200Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.735G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.723G>A
  hgvsp: ENSP00000451460.1:p.Met241Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.600G>A
  hgvsp: ENSP00000351481.4:p.Met200Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.600G>A
  hgvsp: ENSP00000451251.1:p.Met200Ile
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.626G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.600G>A
  hgvsp: ENSP00000451887.1:p.Met200Ile
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met241Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

14-100820032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820032
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820032
    reference: chr 14
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.594C>T
  hgvsp: ENST00000553395.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.594C>T
  hgvsp: ENST00000556645.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.594C>T
  hgvsp: ENST00000556504.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.717C>T
  hgvsp: ENST00000557135.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.717C>T
  hgvsp: ENST00000355338.2:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.620C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.717C>T
  hgvsp: ENST00000392882.2:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.594C>T
  hgvsp: ENST00000344102.5:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-96G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.729C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.594C>T
  hgvsp: ENST00000358655.4:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp239Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

14-100820049-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820049
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820049
    reference: chr 14
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.700A>G
  hgvsp: ENSP00000376620.2:p.Ile234Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.577A>G
  hgvsp: ENSP00000451251.1:p.Ile193Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.700A>G
  hgvsp: ENSP00000347495.2:p.Ile234Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.577A>G
  hgvsp: ENSP00000351481.4:p.Ile193Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.712A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.700A>G
  hgvsp: ENSP00000451460.1:p.Ile234Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.577A>G
  hgvsp: ENSP00000451887.1:p.Ile193Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.577A>G
  hgvsp: ENSP00000339485.5:p.Ile193Val
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-79T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.603A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.577A>G
  hgvsp: ENSP00000451490.1:p.Ile193Val
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile234Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

14-100820079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820079
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820079
    reference: chr 14
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.670G>A
  hgvsp: ENSP00000376620.2:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.547G>A
  hgvsp: ENSP00000451251.1:p.Ala183Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-49C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.547G>A
  hgvsp: ENSP00000339485.5:p.Ala183Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.682G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.670G>A
  hgvsp: ENSP00000347495.2:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.547G>A
  hgvsp: ENSP00000451887.1:p.Ala183Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.573G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.547G>A
  hgvsp: ENSP00000451490.1:p.Ala183Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.547G>A
  hgvsp: ENSP00000351481.4:p.Ala183Thr
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.670G>A
  hgvsp: ENSP00000451460.1:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala224Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-100820080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820080
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820080
    reference: chr 14
allele count: 19
allele frequency: 1.564945226917058e-4
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.546C>T
  hgvsp: ENST00000556504.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.572C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.669C>T
  hgvsp: ENST00000355338.2:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.669C>T
  hgvsp: ENST00000557135.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.546C>T
  hgvsp: ENST00000553395.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.669C>T
  hgvsp: ENST00000392882.2:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.546C>T
  hgvsp: ENST00000344102.5:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.681C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.546C>T
  hgvsp: ENST00000358655.4:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.546C>T
  hgvsp: ENST00000556645.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-48G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Ile223Ile
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: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-100820114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820114
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820114
    reference: chr 14
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.512A>G
  hgvsp: ENSP00000451887.1:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.512A>G
  hgvsp: ENSP00000451490.1:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.538A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.635A>G
  hgvsp: ENSP00000451460.1:p.Tyr212Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.647A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-14T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.512A>G
  hgvsp: ENSP00000351481.4:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.635A>G
  hgvsp: ENSP00000376620.2:p.Tyr212Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.512A>G
  hgvsp: ENSP00000451251.1:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.635A>G
  hgvsp: ENSP00000347495.2:p.Tyr212Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.635A>G
  hgvsp: ENSP00000450500.1:p.Tyr212Cys
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.512A>G
  hgvsp: ENSP00000339485.5:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr212Cys
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

14-100820124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820124
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820124
    reference: chr 14
allele count: 4
allele frequency: 3.294675803900896e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.625G>A
  hgvsp: ENSP00000376620.2:p.Asp209Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.502G>A
  hgvsp: ENSP00000451251.1:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.625G>A
  hgvsp: ENSP00000347495.2:p.Asp209Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.502G>A
  hgvsp: ENSP00000351481.4:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.502G>A
  hgvsp: ENSP00000451887.1:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115-4C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.528G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.502G>A
  hgvsp: ENSP00000339485.5:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.625G>A
  hgvsp: ENSP00000451460.1:p.Asp209Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.637G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.625G>A
  hgvsp: ENSP00000450500.1:p.Asp209Asn
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.502G>A
  hgvsp: ENSP00000451490.1:p.Asp168Asn
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp209Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

14-100820128-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820128
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820128
    reference: chr 14
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.498C>A
  hgvsp: ENST00000556504.1:c.498C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.633C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.621C>A
  hgvsp: ENST00000392882.2:c.621C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.498C>A
  hgvsp: ENST00000556645.1:c.498C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.115G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.621C>A
  hgvsp: ENST00000557722.1:c.621C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.498C>A
  hgvsp: ENST00000344102.5:c.498C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.621C>A
  hgvsp: ENST00000557135.1:c.621C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.524C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.498C>A
  hgvsp: ENST00000358655.4:c.498C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.621C>A
  hgvsp: ENST00000355338.2:c.621C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.498C>A
  hgvsp: ENST00000553395.1:c.498C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.115G>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

14-100820137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820137
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820137
    reference: chr 14
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.612G>A
  hgvsp: ENST00000557722.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.612G>A
  hgvsp: ENST00000355338.2:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.489G>A
  hgvsp: ENST00000556645.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.612G>A
  hgvsp: ENST00000392882.2:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.489G>A
  hgvsp: ENST00000556504.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.124C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.489G>A
  hgvsp: ENST00000344102.5:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.489G>A
  hgvsp: ENST00000358655.4:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.489G>A
  hgvsp: ENST00000553395.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.624G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.515G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.612G>A
  hgvsp: ENST00000557135.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Lys204Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

14-100820155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820155
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820155
    reference: chr 14
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.471C>T
  hgvsp: ENST00000344102.5:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.471C>T
  hgvsp: ENST00000358655.4:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.471C>T
  hgvsp: ENST00000556504.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.594C>T
  hgvsp: ENST00000557135.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.594C>T
  hgvsp: ENST00000355338.2:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.471C>T
  hgvsp: ENST00000553395.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.594C>T
  hgvsp: ENST00000392882.2:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.142G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.606C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.471C>T
  hgvsp: ENST00000556645.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.497C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.594C>T
  hgvsp: ENST00000557722.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp198Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

14-100820161-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820161
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820161
    reference: chr 14
allele count: 5
allele frequency: 4.119226903494752e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.588G>A
  hgvsp: ENST00000392882.2:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.465G>A
  hgvsp: ENST00000553395.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.588G>A
  hgvsp: ENST00000355338.2:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.465G>A
  hgvsp: ENST00000556504.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.600G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.465G>A
  hgvsp: ENST00000344102.5:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.465G>A
  hgvsp: ENST00000556645.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.465G>A
  hgvsp: ENST00000358655.4:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.588G>A
  hgvsp: ENST00000557135.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.148C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.588G>A
  hgvsp: ENST00000557722.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.491G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr196Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

14-100820163-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820163
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820163
    reference: chr 14
allele count: 11
allele frequency: 9.063045842533698e-5
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.463A>G
  hgvsp: ENSP00000339485.5:p.Thr155Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.489A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.586A>G
  hgvsp: ENSP00000451460.1:p.Thr196Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.586A>G
  hgvsp: ENSP00000347495.2:p.Thr196Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.150T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.463A>G
  hgvsp: ENSP00000451887.1:p.Thr155Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.463A>G
  hgvsp: ENSP00000351481.4:p.Thr155Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.598A>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.586A>G
  hgvsp: ENSP00000376620.2:p.Thr196Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.586A>G
  hgvsp: ENSP00000450500.1:p.Thr196Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.463A>G
  hgvsp: ENST00000557297.1:c.463A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.463A>G
  hgvsp: ENSP00000451490.1:p.Thr155Ala
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.463A>G
  hgvsp: ENSP00000451251.1:p.Thr155Ala
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr196Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-100820168-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820168
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820168
    reference: chr 14
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.458A>C
  hgvsp: ENSP00000451251.1:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.581A>C
  hgvsp: ENSP00000450500.1:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.458A>C
  hgvsp: ENSP00000451490.1:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.484A>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.155T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.458A>C
  hgvsp: ENSP00000452519.1:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.581A>C
  hgvsp: ENSP00000347495.2:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.581A>C
  hgvsp: ENSP00000376620.2:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.458A>C
  hgvsp: ENSP00000451599.1:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.581A>C
  hgvsp: ENSP00000451460.1:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.593A>C
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.458A>C
  hgvsp: ENSP00000451887.1:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.458A>C
  hgvsp: ENSP00000339485.5:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.458A>C
  hgvsp: ENSP00000351481.4:p.Gln153Pro
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25208
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln194Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

14-100820184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820184
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820184
    reference: chr 14
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.577G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.442G>A
  hgvsp: ENSP00000339485.5:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.565G>A
  hgvsp: ENSP00000451460.1:p.Val189Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.442G>A
  hgvsp: ENSP00000451887.1:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.565G>A
  hgvsp: ENSP00000347495.2:p.Val189Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.442G>A
  hgvsp: ENSP00000452519.1:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.468G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.565G>A
  hgvsp: ENSP00000450500.1:p.Val189Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.565G>A
  hgvsp: ENSP00000376620.2:p.Val189Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.442G>A
  hgvsp: ENSP00000351481.4:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.442G>A
  hgvsp: ENSP00000451490.1:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.442G>A
  hgvsp: ENSP00000451251.1:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.442G>A
  hgvsp: ENSP00000451599.1:p.Val148Met
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.171C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val189Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

14-100820184-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820184
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820183
    reference: chr 14
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.441delC
  hgvsp: ENSP00000451251.1:p.Asn147LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.172delG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.564delC
  hgvsp: ENSP00000376620.2:p.Asn188LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.441delC
  hgvsp: ENSP00000339485.5:p.Asn147LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.564delC
  hgvsp: ENSP00000347495.2:p.Asn188LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.441delC
  hgvsp: ENSP00000451599.1:p.Asn147LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.441delC
  hgvsp: ENSP00000451490.1:p.Asn147LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.441delC
  hgvsp: ENSP00000452519.1:p.Asn147LysfsTer?
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.441delC
  hgvsp: ENSP00000451887.1:p.Asn147LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.467delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.564delC
  hgvsp: ENSP00000451460.1:p.Asn188LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.564delC
  hgvsp: ENSP00000450500.1:p.Asn188LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.576delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.441delC
  hgvsp: ENSP00000351481.4:p.Asn147LysfsTer8
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn188LysfsTer8
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: CG
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

14-100820188-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820188
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820188
    reference: chr 14
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.438T>A
  hgvsp: ENSP00000339485.5:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.438T>A
  hgvsp: ENSP00000452519.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.561T>A
  hgvsp: ENSP00000450500.1:p.Phe187Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.438T>A
  hgvsp: ENSP00000451490.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.561T>A
  hgvsp: ENSP00000376620.2:p.Phe187Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.573T>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.464T>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.561T>A
  hgvsp: ENSP00000347495.2:p.Phe187Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.438T>A
  hgvsp: ENSP00000451251.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.438T>A
  hgvsp: ENSP00000451599.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.175A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.438T>A
  hgvsp: ENSP00000451887.1:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.438T>A
  hgvsp: ENSP00000351481.4:p.Phe146Leu
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.561T>A
  hgvsp: ENSP00000451460.1:p.Phe187Leu
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe187Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

14-100820206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820206
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820206
    reference: chr 14
allele count: 1
allele frequency: 8.291598951941893e-6
allele num: 120604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420G>A
  hgvsp: ENST00000358655.4:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543G>A
  hgvsp: ENST00000557135.1:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420G>A
  hgvsp: ENST00000556435.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543G>A
  hgvsp: ENST00000557722.1:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.193C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420G>A
  hgvsp: ENST00000556504.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420G>A
  hgvsp: ENST00000553395.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420G>A
  hgvsp: ENST00000344102.5:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543G>A
  hgvsp: ENST00000355338.2:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420G>A
  hgvsp: ENST00000557297.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543G>A
  hgvsp: ENST00000392882.2:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.555G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420G>A
  hgvsp: ENST00000556645.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.543G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/14-100820218-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820218
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820218
    reference: chr 14
allele count: 5
allele frequency: 4.169724464607379e-5
allele num: 119912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.205C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.543G>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-12G>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23966
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13574
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-100820219-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820219
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820218
    reference: chr 14
allele count: 5
allele frequency: 4.175853544464488e-5
allele num: 119736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.541delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.211delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-14delC
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: AG
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

14-100820220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820220
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820220
    reference: chr 14
allele count: 3
allele frequency: 2.505972567953623e-5
allele num: 119714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.207G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-14C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.541C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-14C>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-100820221-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820221
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820221
    reference: chr 14
allele count: 5
allele frequency: 4.176551171104949e-5
allele num: 119716
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.208G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.540C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-15C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-15C>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

14-100820230-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820230
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820230
    reference: chr 14
allele count: 3
allele frequency: 2.519695620769011e-5
allele num: 119062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.531C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.217G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-24C>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-24C>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

14-100820231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820231
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820231
    reference: chr 14
allele count: 1
allele frequency: 8.406328283932143e-6
allele num: 118958
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.530G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.218C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-25G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-25G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11345
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

14-100820233-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820233
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820233
    reference: chr 14
allele count: 1
allele frequency: 8.41283462049703e-6
allele num: 118866
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.220G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.528C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-27C>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-27C>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

14-100820235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820235
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820235
    reference: chr 14
allele count: 2
allele frequency: 1.68625533278249e-5
allele num: 118606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.222C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.526G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-29G>A
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-29G>A
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

14-100820236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820236
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820236
    reference: chr 14
allele count: 9
allele frequency: 7.587381341786239e-5
allele num: 118618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.223G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.525C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-30C>T
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19328
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10001
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-100820241-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820241
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820241
    reference: chr 14
allele count: 13
allele frequency: 1.098473966167002e-4
allele num: 118346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.520T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.228A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-35T>G
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8173
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8933
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17278
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

14-100820244-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 100820244
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 100820243
    reference: chr 14
allele count: 1
allele frequency: 8.474863554696769e-6
allele num: 117996
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000347495
  ensembl transcript: ENST00000355338
  gene symbol: WARS
  hgvsc: ENST00000355338.2:c.543-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000452519
  ensembl transcript: ENST00000556435
  gene symbol: WARS
  hgvsc: ENST00000556435.1:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451599
  ensembl transcript: ENST00000557297
  gene symbol: WARS
  hgvsc: ENST00000557297.1:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451460
  ensembl transcript: ENST00000557135
  gene symbol: WARS
  hgvsc: ENST00000557135.1:c.543-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554084
  gene symbol: WARS
  hgvsc: ENST00000554084.1:n.446-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000351481
  ensembl transcript: ENST00000358655
  gene symbol: WARS
  hgvsc: ENST00000358655.4:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000450500
  ensembl transcript: ENST00000557722
  gene symbol: WARS
  hgvsc: ENST00000557722.1:c.543-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451490
  ensembl transcript: ENST00000553395
  gene symbol: WARS
  hgvsc: ENST00000553395.1:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140105
  ensembl transcript: ENST00000554950
  gene symbol: WARS
  hgvsc: ENST00000554950.1:n.516delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000258666
  ensembl transcript: ENST00000557226
  gene symbol: RP11-638I2.8
  hgvsc: ENST00000557226.1:n.235delC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451251
  ensembl transcript: ENST00000556504
  gene symbol: WARS
  hgvsc: ENST00000556504.1:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000376620
  ensembl transcript: ENST00000392882
  gene symbol: WARS
  hgvsc: ENST00000392882.2:c.543-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000339485
  ensembl transcript: ENST00000344102
  gene symbol: WARS
  hgvsc: ENST00000344102.5:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140105
  ensembl protein: ENSP00000451887
  ensembl transcript: ENST00000556645
  gene symbol: WARS
  hgvsc: ENST00000556645.1:c.420-39delG
  variant of: http://identifiers.org/hgnc/12729
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8313
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: TC

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6312
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19623
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 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: 11556
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.143362e6

QD
type: SiteQuality
SIO_000300: 1.637e1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 2.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

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

GenotypeQuality
all individuals: 3835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12815
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19623
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6312
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
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: 11556
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.122e0

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.637e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

DP
type: SiteQuality
SIO_000300: 2.143362e6

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6315
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19643
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

DP
type: SiteQuality
SIO_000300: 2.144642e6

QD
type: SiteQuality
SIO_000300: 1.264e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.092e0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 12

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 31

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 64

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2485
bin: 6.25e1
variant carriers: 150

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 33

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 24

GenotypeQuality
all individuals: 356
bin: 7.25e1
variant carriers: 164

GenotypeQuality
all individuals: 663
bin: 9.25e1
variant carriers: 551

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 707
bin: 6.75e1
variant carriers: 193

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 83

GenotypeQuality
all individuals: 550
bin: 7.75e1
variant carriers: 309

GenotypeQuality
all individuals: 54543
bin: 9.75e1
variant carriers: 53992

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 76

European (Non-Finnish)
type: Population
allele count: 49751
allele frequency: 7.462500749985e-1
allele num: 66668
num of homozygotes: 18642

Other
type: Population
allele count: 714
allele frequency: 7.880794701986755e-1
allele num: 906
num of homozygotes: 283

African
type: Population
allele count: 5276
allele frequency: 5.076005387723687e-1
allele num: 10394
num of homozygotes: 1332

European (Finnish)
type: Population
allele count: 5193
allele frequency: 7.863416111447608e-1
allele num: 6604
num of homozygotes: 2034

Latino
type: Population
allele count: 10077
allele frequency: 8.715620134924753e-1
allele num: 11562
num of homozygotes: 4414

East Asian
type: Population
allele count: 6786
allele frequency: 7.85234899328859e-1
allele num: 8642
num of homozygotes: 2679

South Asian
type: Population
allele count: 13326
allele frequency: 8.072449721347226e-1
allele num: 16508
num of homozygotes: 5374

QD
type: SiteQuality
SIO_000300: 2.658e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 6.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.592574e6

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

GenotypeQuality
all individuals: 1077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34440
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8185
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2714
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6366
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.975713e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.414e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 9.355e0

VQSLOD
type: SiteQuality
SIO_000300: -4.583e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

QD
type: SiteQuality
SIO_000300: 1.226e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.799046505352163e-4
allele num: 66702
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.852e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.514e0

DP
type: SiteQuality
SIO_000300: 1.975755e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.223e1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2710
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variant carriers: 0

GenotypeQuality
all individuals: 34614
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.975364e6

VQSLOD
type: SiteQuality
SIO_000300: -9.872e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.604e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.96e-1

QD
type: SiteQuality
SIO_000300: 3.495e1

MQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-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
all individuals: 1552
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GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.975103e6

QD
type: SiteQuality
SIO_000300: 9.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.051e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 20
bin: 4.25e1
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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 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: 11568
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.98e-1

FS
type: SiteQuality
SIO_000300: 5.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.552e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.48e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.974993e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 34753
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

DP
type: SiteQuality
SIO_000300: 1.97504e6

QD
type: SiteQuality
SIO_000300: 2.53e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

FS
type: SiteQuality
SIO_000300: 4.686e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.067e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 63

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2438
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 55
allele frequency: 5.289478745912676e-3
allele num: 10398
num of homozygotes: 0

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

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

European (Finnish)
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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: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.995502248875562e-5
allele num: 66700
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.243e1

BaseQRankSum
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SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 1.976767e6

GenotypeDepth
all individuals: 169
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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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GenotypeQuality
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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: 2

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: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
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ReadPosRankSum
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FS
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MQ
type: SiteQuality
SIO_000300: 5.912e1

VQSLOD
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.033e1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
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South Asian
type: Population
allele count: 5
allele frequency: 3.028467595396729e-4
allele num: 16510
num of homozygotes: 0

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

InbreedingCoeff
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QD
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FS
type: SiteQuality
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DP
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SIO_000300: 1.972689e6

BaseQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

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

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

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

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

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

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

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

South Asian
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MQRankSum
type: SiteQuality
SIO_000300: 9.04e-1

ClippingRankSum
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BaseQRankSum
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MQ
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FS
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DP
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InbreedingCoeff
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 5.34e0

ReadPosRankSum
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SIO_000300: 9.7e-2

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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SIO_000300: -7.63e-1

ClippingRankSum
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SIO_000300: 2.22e-1

ReadPosRankSum
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FS
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DP
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele num: 6612
num of homozygotes: 0

South Asian
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East Asian
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African
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Latino
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VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

InbreedingCoeff
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QD
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DP
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

Other
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African
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South Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -6.95e-1

ReadPosRankSum
type: SiteQuality
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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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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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QD
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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allele num: 66260
num of homozygotes: 0

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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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

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

South Asian
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allele count: 87
allele frequency: 5.288753799392097e-3
allele num: 16450
num of homozygotes: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510345869204048e-5
allele num: 66210
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.264e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.98e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

DP
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SIO_000300: 1.931742e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

FS
type: SiteQuality
SIO_000300: 8.88e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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bin: 9.75e1
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.531995890990392e-5
allele num: 66196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.159e1

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

FS
type: SiteQuality
SIO_000300: 5.72e0

DP
type: SiteQuality
SIO_000300: 1.926617e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.351e0

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 1.66e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 1.923215e6

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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.057169061449098e-4
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.049524274213223e-5
allele num: 65584
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

DP
type: SiteQuality
SIO_000300: 1.781478e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeQuality
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bin: 5.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2414
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.102770657878677e-5
allele num: 16386
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.390057361376673e-4
allele num: 8368
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.781478e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.531205977828137e-5
allele num: 65308
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.811616954474098e-5
allele num: 10192
num of homozygotes: 0

South Asian
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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: 8258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.63e-1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: -1.323e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 2.433682161109759e-4
allele num: 8218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534354190321294e-5
allele num: 65174
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.830908375933936e-5
allele num: 10172
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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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European (Non-Finnish)
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allele count: 1
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allele num: 65122
num of homozygotes: 0

South Asian
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East Asian
type: Population
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Other
type: Population
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allele frequency: 1.123595505617978e-3
allele num: 890
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European (Finnish)
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allele num: 6502
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African
type: Population
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Latino
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VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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QD
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FS
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MQ
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ReadPosRankSum
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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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.069085105729982e-5
allele num: 65166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

DP
type: SiteQuality
SIO_000300: 1.691213e6

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.463e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.53e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
all individuals: 2053
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2243
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 183
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2645
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1879
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4550
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5134
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1959
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1447
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 938
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18061
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2345
bin: 2.75e1
variant carriers: 2

Latino
type: Population
allele count: 37
allele frequency: 3.288304301457519e-3
allele num: 11252
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.257336343115124e-3
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 64
allele frequency: 3.917727717923604e-3
allele num: 16336
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 51
allele frequency: 7.826887661141806e-3
allele num: 6516
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8206
num of homozygotes: 0

African
type: Population
allele count: 319
allele frequency: 3.135443286809515e-2
allele num: 10174
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 408
allele frequency: 6.260933615689163e-3
allele num: 65166
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

DP
type: SiteQuality
SIO_000300: 1.691213e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

QD
type: SiteQuality
SIO_000300: 1.463e1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.53e0

GenotypeQuality
all individuals: 4309
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4892
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15700
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5994
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537941004583064e-5
allele num: 65022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.670442e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

GenotypeQuality
all individuals: 4009
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4498
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variant carriers: 0

GenotypeQuality
all individuals: 1466
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5258
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variant carriers: 0

GenotypeQuality
all individuals: 2600
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variant carriers: 0

GenotypeQuality
all individuals: 3167
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variant carriers: 0

GenotypeQuality
all individuals: 5037
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variant carriers: 0

GenotypeQuality
all individuals: 11488
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variant carriers: 0

GenotypeQuality
all individuals: 5992
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1780
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5677
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variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.097413659594239e-5
allele num: 64570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8084
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.546e0

QD
type: SiteQuality
SIO_000300: 1.286e1

DP
type: SiteQuality
SIO_000300: 1.646367e6

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 120
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4765
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 791
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1285
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9179
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 7.75e1
variant carriers: 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: 10374
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.122145528628334e-5
allele num: 65774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14630
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.618e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

QD
type: SiteQuality
SIO_000300: 1.608e1

DP
type: SiteQuality
SIO_000300: 1.797174e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

VQSLOD
type: SiteQuality
SIO_000300: 3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

GenotypeQuality
all individuals: 9176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30716
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
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: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.870019236053861e-5
allele num: 14556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65742
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.916e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

DP
type: SiteQuality
SIO_000300: 1.797619e6

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.469e0

VQSLOD
type: SiteQuality
SIO_000300: -1.661e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.67e-1

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2908
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65900
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.275e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.812832e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeQuality
all individuals: 3630
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
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GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 4727
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variant carriers: 1

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.45577792123951e-5
allele num: 15490
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.194e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 7.611e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQ
type: SiteQuality
SIO_000300: 5.89e1

QD
type: SiteQuality
SIO_000300: 1.155e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.831349e6

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34353
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variant carriers: 0

GenotypeQuality
all individuals: 4728
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2222
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
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GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9370
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.845414343395501e-4
allele num: 10402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66292
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.413e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.158e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.836983e6

QD
type: SiteQuality
SIO_000300: 1.207e1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 12

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: 5.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507431637975218e-5
allele num: 66338
num of homozygotes: 0

African
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allele count: 10
allele frequency: 9.615384615384616e-4
allele num: 10400
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15846
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.839802e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.35e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 2.705e0

QD
type: SiteQuality
SIO_000300: 1.154e1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.71e-1

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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variant carriers: 25

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9392
bin: 6.75e1
variant carriers: 0

Latino
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allele count: 6
allele frequency: 5.184929139301763e-4
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
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allele count: 4
allele frequency: 3.846153846153846e-4
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.248437890527369e-5
allele num: 16004
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.108052761549118e-4
allele num: 66412
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-1

DP
type: SiteQuality
SIO_000300: 1.842271e6

QD
type: SiteQuality
SIO_000300: 1.308e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeDepth
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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
all individuals: 2927
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variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

DP
type: SiteQuality
SIO_000300: 1.846712e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.021e1

QD
type: SiteQuality
SIO_000300: 1.287e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.226e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 97
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variant carriers: 0

GenotypeDepth
all individuals: 930
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 2925
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GenotypeQuality
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
all individuals: 26
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4696
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 904
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GenotypeQuality
all individuals: 9431
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.850037e6

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

FS
type: SiteQuality
SIO_000300: 9.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

QD
type: SiteQuality
SIO_000300: 1.308e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2933
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.15e-2

DP
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BaseQRankSum
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SIO_000300: -3.09e0

ReadPosRankSum
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QD
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
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FS
type: SiteQuality
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VQSLOD
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SIO_000300: 1.2e0

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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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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East Asian
type: Population
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Other
type: Population
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FS
type: SiteQuality
SIO_000300: 3.226e0

ReadPosRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 8.23e-1

BaseQRankSum
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VQSLOD
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InbreedingCoeff
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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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bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

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

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

FS
type: SiteQuality
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MQ
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QD
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 17
allele frequency: 2.547274416374479e-4
allele num: 66738
num of homozygotes: 0

East Asian
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Other
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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FS
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BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11578
num of homozygotes: 0

Other
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South Asian
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East Asian
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European (Non-Finnish)
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allele num: 66740
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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African
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Other
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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African
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Other
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South Asian
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East Asian
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European (Finnish)
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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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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QD
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BaseQRankSum
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DP
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 11
allele frequency: 9.502418797512094e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

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

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

FS
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SIO_000300: 2.341e0

InbreedingCoeff
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SIO_000300: 1.7e-2

ClippingRankSum
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DP
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MQ
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SIO_000300: 5.942e1

QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 1.23e-2

VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 8.159999999999999e-1

QD
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ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele count: 0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66640
num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.563838799467505e-5
allele num: 66104
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15932
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
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SIO_000300: 5.89e1

BaseQRankSum
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SIO_000300: -2.906e0

ClippingRankSum
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MQRankSum
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QD
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FS
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SIO_000300: 3.323e0

ReadPosRankSum
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SIO_000300: 4.01e-1

VQSLOD
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DP
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SIO_000300: 1.801733e6

GenotypeDepth
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66016
num of homozygotes: 0

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

East Asian
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allele count: 5
allele frequency: 5.852059925093633e-4
allele num: 8544
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -5.0e-4

DP
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FS
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QD
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MQRankSum
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SIO_000300: 9.64e-1

ReadPosRankSum
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SIO_000300: 5.45e-1

ClippingRankSum
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SIO_000300: 3.84e-1

VQSLOD
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SIO_000300: 2.77e0

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

Latino
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allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.936483346243222e-4
allele num: 10328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66018
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

QD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
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SIO_000300: 7.708e0

DP
type: SiteQuality
SIO_000300: 1.787938e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
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SIO_000300: -5.28e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.14821810855056e-4
allele num: 15882
num of homozygotes: 1

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: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 1.08e0

ReadPosRankSum
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SIO_000300: 1.2e0

InbreedingCoeff
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BaseQRankSum
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DP
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SIO_000300: 1.787263e6

MQRankSum
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SIO_000300: -3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.234e-1

QD
type: SiteQuality
SIO_000300: 1.893e1

GenotypeDepth
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
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

Latino
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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
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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 (Non-Finnish)
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allele count: 3
allele frequency: 4.568991775814804e-5
allele num: 65660
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

FS
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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DP
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SIO_000300: 1.712556e6

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.947e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523786304208698e-5
allele num: 65626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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QD
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
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
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num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52452968259292e-5
allele num: 65594
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

DP
type: SiteQuality
SIO_000300: 1.68132e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

QD
type: SiteQuality
SIO_000300: 1.688e1

GenotypeDepth
all individuals: 8088
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5727
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3076
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 705
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4556
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2496
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.77963125548727e-5
allele num: 11390
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.725734292939116e-5
allele num: 10282
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

QD
type: SiteQuality
SIO_000300: 6.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.658163e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.876e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

GenotypeDepth
all individuals: 5697
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 591
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3073
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4557
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2473
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2014
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.282380097460887e-4
allele num: 15596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.163103237629811e-5
allele num: 65480
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.655727e6

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.355e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 3.905e0

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeDepth
all individuals: 245
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 590
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3802
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 431
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6569
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4985
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22309
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2352
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4547
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 3024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.060537430372773e-5
allele num: 65348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 7.085802628188611e-4
allele num: 15524
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.704e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

DP
type: SiteQuality
SIO_000300: 1.615056e6

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1