11-3040330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040330
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040330
    reference: chr 11
allele count: 18
allele frequency: 1.623083859332732e-4
allele num: 110900
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3404+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1055+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1185+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1146+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1116+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*964+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1395+39A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1146+39A>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-3040345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040345
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040345
    reference: chr 11
allele count: 1
allele frequency: 9.008684371734351e-6
allele num: 111004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1146+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1146+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3404+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1055+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1395+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*964+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1185+24G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1116+24G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

11-3040348-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040348
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040348
    reference: chr 11
allele count: 1
allele frequency: 9.006412565746812e-6
allele num: 111032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1146+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1185+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*964+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3404+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1395+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1055+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1116+21C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1146+21C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47291
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-3040349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040349
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040349
    reference: chr 11
allele count: 1
allele frequency: 9.004304057339408e-6
allele num: 111058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1116+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1185+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*964+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1055+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3404+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1146+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1146+20C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1395+20C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47291
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3413
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

11-3040350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040350
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040350
    reference: chr 11
allele count: 1
allele frequency: 9.002358617957905e-6
allele num: 111082
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1395+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1116+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1185+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1055+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1146+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1146+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3404+19C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*964+19C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

11-3040361-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040361
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040361
    reference: chr 11
allele count: 1
allele frequency: 8.993291004910338e-6
allele num: 111194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1146+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*964+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1395+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1146+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1055+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3404+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1116+8A>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1185+8A>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 9.25e1
  variant carriers: 0
hgvs: c.1395+8A>C
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-3040372-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040372
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040372
    reference: chr 11
allele count: 1
allele frequency: 8.981336782166658e-6
allele num: 111342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1113G>C
  hgvsp: ENST00000397114.3:c.1113G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*961G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1143G>C
  hgvsp: ENST00000397111.5:c.1143G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1052G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1143G>C
  hgvsp: ENST00000278224.9:c.1143G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1392G>C
  hgvsp: ENST00000380525.4:c.1392G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1182G>C
  hgvsp: ENST00000401769.3:c.1182G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3401G>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser464Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-3040372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040372
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040372
    reference: chr 11
allele count: 13
allele frequency: 1.167573781681665e-4
allele num: 111342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*961G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1182G>A
  hgvsp: ENST00000401769.3:c.1182G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1143G>A
  hgvsp: ENST00000397111.5:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1143G>A
  hgvsp: ENST00000278224.9:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1052G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1113G>A
  hgvsp: ENST00000397114.3:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1392G>A
  hgvsp: ENST00000380525.4:c.1392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3401G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47290
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser464Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-3040373-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040373
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040373
    reference: chr 11
allele count: 1
allele frequency: 8.97778895013736e-6
allele num: 111386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*960C>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3400C>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1051C>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1142C>A
  hgvsp: ENSP00000278224.9:p.Ser381Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1391C>A
  hgvsp: ENSP00000369897.4:p.Ser464Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1112C>A
  hgvsp: ENSP00000380303.3:p.Ser371Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1142C>A
  hgvsp: ENSP00000380300.5:p.Ser381Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1181C>A
  hgvsp: ENSP00000384069.3:p.Ser394Ter
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3544
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser464Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

11-3040377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040377
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040377
    reference: chr 11
allele count: 1
allele frequency: 8.970701688286057e-6
allele num: 111474
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1387C>T
  hgvsp: ENSP00000369897.4:p.Gln463Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*956C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1138C>T
  hgvsp: ENSP00000380300.5:p.Gln380Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1177C>T
  hgvsp: ENSP00000384069.3:p.Gln393Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1108C>T
  hgvsp: ENSP00000380303.3:p.Gln370Ter
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1047C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3396C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1138C>T
  hgvsp: ENSP00000278224.9:p.Gln380Ter
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln463Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-3040380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040380
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040380
    reference: chr 11
allele count: 1
allele frequency: 8.970057946574335e-6
allele num: 111482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3393G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1044G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1174G>T
  hgvsp: ENSP00000384069.3:p.Ala392Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1135G>T
  hgvsp: ENSP00000380300.5:p.Ala379Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1135G>T
  hgvsp: ENSP00000278224.9:p.Ala379Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1105G>T
  hgvsp: ENSP00000380303.3:p.Ala369Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1384G>T
  hgvsp: ENSP00000369897.4:p.Ala462Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*953G>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3504
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala462Ser
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-3040388-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040388
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040388
    reference: chr 11
allele count: 3
allele frequency: 2.686390744488422e-5
allele num: 111674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1127A>G
  hgvsp: ENSP00000278224.9:p.Asn376Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1166A>G
  hgvsp: ENSP00000384069.3:p.Asn389Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1376A>G
  hgvsp: ENSP00000369897.4:p.Asn459Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3385A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1127A>G
  hgvsp: ENSP00000380300.5:p.Asn376Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1097A>G
  hgvsp: ENSP00000380303.3:p.Asn366Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1036A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*945A>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47288
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn459Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-3040396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040396
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040396
    reference: chr 11
allele count: 1
allele frequency: 8.94566403664144e-6
allele num: 111786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*937C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1368C>T
  hgvsp: ENST00000380525.4:c.1368C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1119C>T
  hgvsp: ENST00000397111.5:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1119C>T
  hgvsp: ENST00000278224.9:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1158C>T
  hgvsp: ENST00000401769.3:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1028C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3377C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1089C>T
  hgvsp: ENST00000397114.3:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His456His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-3040398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040398
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040398
    reference: chr 11
allele count: 1
allele frequency: 8.947264821144176e-6
allele num: 111766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1117C>T
  hgvsp: ENSP00000278224.9:p.His373Tyr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1087C>T
  hgvsp: ENSP00000380303.3:p.His363Tyr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1026C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1156C>T
  hgvsp: ENSP00000384069.3:p.His386Tyr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*935C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1366C>T
  hgvsp: ENSP00000369897.4:p.His456Tyr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3375C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1117C>T
  hgvsp: ENSP00000380300.5:p.His373Tyr
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47285
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3572
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His456Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

11-3040399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040399
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040399
    reference: chr 11
allele count: 1
allele frequency: 8.946784525641484e-6
allele num: 111772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1116C>T
  hgvsp: ENST00000278224.9:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1116C>T
  hgvsp: ENST00000397111.5:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3374C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1155C>T
  hgvsp: ENST00000401769.3:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1086C>T
  hgvsp: ENST00000397114.3:c.1086C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1365C>T
  hgvsp: ENST00000380525.4:c.1365C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1025C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*934C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro455Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-3040402-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040402
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040402
    reference: chr 11
allele count: 13
allele frequency: 1.162686700652893e-4
allele num: 111810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1152C>T
  hgvsp: ENST00000401769.3:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1022C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1113C>T
  hgvsp: ENST00000278224.9:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1362C>T
  hgvsp: ENST00000380525.4:c.1362C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3371C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1113C>T
  hgvsp: ENST00000397111.5:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1083C>T
  hgvsp: ENST00000397114.3:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*931C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe454Phe
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

11-3040410-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040410
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040410
    reference: chr 11
allele count: 1
allele frequency: 8.937668698496684e-6
allele num: 111886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1105C>T
  hgvsp: ENSP00000278224.9:p.Leu369Phe
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1014C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1144C>T
  hgvsp: ENSP00000384069.3:p.Leu382Phe
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1354C>T
  hgvsp: ENSP00000369897.4:p.Leu452Phe
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*923C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1075C>T
  hgvsp: ENSP00000380303.3:p.Leu359Phe
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3363C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1105C>T
  hgvsp: ENSP00000380300.5:p.Leu369Phe
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47282
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu452Phe
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

11-3040414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040414
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040414
    reference: chr 11
allele count: 2
allele frequency: 1.786448005430802e-5
allele num: 111954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1140C>T
  hgvsp: ENST00000401769.3:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1101C>T
  hgvsp: ENST00000397111.5:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1350C>T
  hgvsp: ENST00000380525.4:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3359C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1010C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1071C>T
  hgvsp: ENST00000397114.3:c.1071C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*919C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1101C>T
  hgvsp: ENST00000278224.9:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe450Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-3040417-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040417
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040417
    reference: chr 11
allele count: 2
allele frequency: 1.786097020790169e-5
allele num: 111976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1137G>T
  hgvsp: ENST00000401769.3:c.1137G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1098G>T
  hgvsp: ENST00000397111.5:c.1098G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1347G>T
  hgvsp: ENST00000380525.4:c.1347G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*916G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*1007G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1068G>T
  hgvsp: ENST00000397114.3:c.1068G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1098G>T
  hgvsp: ENST00000278224.9:c.1098G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3356G>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly449Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-3040425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040425
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040425
    reference: chr 11
allele count: 1
allele frequency: 8.926977325477594e-6
allele num: 112020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1090G>A
  hgvsp: ENSP00000380300.5:p.Gly364Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1060G>A
  hgvsp: ENSP00000380303.3:p.Gly354Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.653G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*999G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*908G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3348G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1090G>A
  hgvsp: ENSP00000278224.9:p.Gly364Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1129G>A
  hgvsp: ENSP00000384069.3:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1339G>A
  hgvsp: ENSP00000369897.4:p.Gly447Arg
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3520
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly447Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-3040426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040426
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040426
    reference: chr 11
allele count: 1
allele frequency: 8.923790826343031e-6
allele num: 112060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1059C>T
  hgvsp: ENST00000397114.3:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1338C>T
  hgvsp: ENST00000380525.4:c.1338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*998C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1128C>T
  hgvsp: ENST00000401769.3:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.652C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1089C>T
  hgvsp: ENST00000278224.9:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3347C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1089C>T
  hgvsp: ENST00000397111.5:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*907C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His446His
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-3040432-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040432
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040432
    reference: chr 11
allele count: 5
allele frequency: 4.465162799835682e-5
allele num: 111978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1053C>T
  hgvsp: ENST00000397114.3:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1122C>T
  hgvsp: ENST00000401769.3:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3341C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*992C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1332C>T
  hgvsp: ENST00000380525.4:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1083C>T
  hgvsp: ENST00000278224.9:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*901C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.646C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1083C>T
  hgvsp: ENST00000397111.5:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp444Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-3040438-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040438
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040438
    reference: chr 11
allele count: 1
allele frequency: 8.933037947545201e-6
allele num: 111944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.640G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*986G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1077G>T
  hgvsp: ENST00000278224.9:c.1077G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1047G>T
  hgvsp: ENST00000397114.3:c.1047G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1326G>T
  hgvsp: ENST00000380525.4:c.1326G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*895G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1116G>T
  hgvsp: ENST00000401769.3:c.1116G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3335G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1077G>T
  hgvsp: ENST00000397111.5:c.1077G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser442Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

11-3040438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040438
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040438
    reference: chr 11
allele count: 35
allele frequency: 3.12656328164082e-4
allele num: 111944
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1326G>A
  hgvsp: ENST00000380525.4:c.1326G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1077G>A
  hgvsp: ENST00000397111.5:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.640G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1116G>A
  hgvsp: ENST00000401769.3:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3335G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1047G>A
  hgvsp: ENST00000397114.3:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*986G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1077G>A
  hgvsp: ENST00000278224.9:c.1077G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*895G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47263
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser442Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

11-3040439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040439
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040439
    reference: chr 11
allele count: 3
allele frequency: 2.680581864970156e-5
allele num: 111916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1046C>T
  hgvsp: ENSP00000380303.3:p.Ser349Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3334C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1076C>T
  hgvsp: ENSP00000278224.9:p.Ser359Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.639C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*894C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*985C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1325C>T
  hgvsp: ENSP00000369897.4:p.Ser442Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1115C>T
  hgvsp: ENSP00000384069.3:p.Ser372Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1076C>T
  hgvsp: ENSP00000380300.5:p.Ser359Leu
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3940
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser442Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

11-3040449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040449
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040449
    reference: chr 11
allele count: 1
allele frequency: 8.94358387292956e-6
allele num: 111812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*975C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1315C>T
  hgvsp: ENST00000380525.4:c.1315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3324C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1066C>T
  hgvsp: ENST00000397111.5:c.1066C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1036C>T
  hgvsp: ENST00000397114.3:c.1036C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1105C>T
  hgvsp: ENST00000401769.3:c.1105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*884C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.629C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1066C>T
  hgvsp: ENST00000278224.9:c.1066C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu439Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-3040450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040450
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040450
    reference: chr 11
allele count: 5
allele frequency: 4.473872584108804e-5
allele num: 111760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1065C>T
  hgvsp: ENST00000397111.5:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3323C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1104C>T
  hgvsp: ENST00000401769.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1065C>T
  hgvsp: ENST00000278224.9:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*974C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1035C>T
  hgvsp: ENST00000397114.3:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.628C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1314C>T
  hgvsp: ENST00000380525.4:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*883C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3183
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu438Leu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

11-3040453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040453
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040453
    reference: chr 11
allele count: 1
allele frequency: 8.949346697691069e-6
allele num: 111740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1062C>T
  hgvsp: ENST00000278224.9:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.625C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1062C>T
  hgvsp: ENST00000397111.5:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1101C>T
  hgvsp: ENST00000401769.3:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3320C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*880C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1032C>T
  hgvsp: ENST00000397114.3:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*971C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1311C>T
  hgvsp: ENST00000380525.4:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr437Thr
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-3040454-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040454
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040454
    reference: chr 11
allele count: 7
allele frequency: 6.266673828579613e-5
allele num: 111702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1061C>A
  hgvsp: ENSP00000278224.9:p.Thr354Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1100C>A
  hgvsp: ENSP00000384069.3:p.Thr367Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3319C>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1310C>A
  hgvsp: ENSP00000369897.4:p.Thr437Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*970C>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1031C>A
  hgvsp: ENSP00000380303.3:p.Thr344Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.624C>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1061C>A
  hgvsp: ENSP00000380300.5:p.Thr354Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*879C>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr437Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

11-3040463-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040463
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040463
    reference: chr 11
allele count: 1
allele frequency: 8.968931620865323e-6
allele num: 111496
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1301T>C
  hgvsp: ENSP00000369897.4:p.Met434Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1052T>C
  hgvsp: ENSP00000380300.5:p.Met351Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1022T>C
  hgvsp: ENSP00000380303.3:p.Met341Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.615T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1052T>C
  hgvsp: ENSP00000278224.9:p.Met351Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*961T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1091T>C
  hgvsp: ENSP00000384069.3:p.Met364Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3310T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*870T>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met434Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-3040464-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040464
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040464
    reference: chr 11
allele count: 1
allele frequency: 8.969897025582147e-6
allele num: 111484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*869A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3309A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1021A>G
  hgvsp: ENSP00000380303.3:p.Met341Val
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1090A>G
  hgvsp: ENSP00000384069.3:p.Met364Val
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.614A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*960A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1300A>G
  hgvsp: ENSP00000369897.4:p.Met434Val
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1051A>G
  hgvsp: ENSP00000380300.5:p.Met351Val
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1051A>G
  hgvsp: ENSP00000278224.9:p.Met351Val
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met434Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

11-3040468-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040468
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040468
    reference: chr 11
allele count: 2
allele frequency: 1.796783757074836e-5
allele num: 111310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*956G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1047G>A
  hgvsp: ENST00000278224.9:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1017G>A
  hgvsp: ENST00000397114.3:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1047G>A
  hgvsp: ENST00000397111.5:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1086G>A
  hgvsp: ENST00000401769.3:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.610G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3305G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*865G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1296G>A
  hgvsp: ENST00000380525.4:c.1296G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3722
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser432Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

11-3040470-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040470
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040470
    reference: chr 11
allele count: 1
allele frequency: 8.985856262243229e-6
allele num: 111286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1084T>C
  hgvsp: ENSP00000384069.3:p.Ser362Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1015T>C
  hgvsp: ENSP00000380303.3:p.Ser339Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.608T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1045T>C
  hgvsp: ENSP00000278224.9:p.Ser349Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1294T>C
  hgvsp: ENSP00000369897.4:p.Ser432Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*954T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1045T>C
  hgvsp: ENSP00000380300.5:p.Ser349Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*863T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3303T>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47252
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser432Pro
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

11-3040477-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040477
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040477
    reference: chr 11
allele count: 5
allele frequency: 4.502314189493399e-5
allele num: 111054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.601C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.1008C>T
  hgvsp: ENST00000397114.3:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1287C>T
  hgvsp: ENST00000380525.4:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3296C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*856C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1038C>T
  hgvsp: ENST00000397111.5:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*947C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1077C>T
  hgvsp: ENST00000401769.3:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1038C>T
  hgvsp: ENST00000278224.9:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile429Ile
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

11-3040489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040489
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040489
    reference: chr 11
allele count: 3
allele frequency: 2.720101550457884e-5
allele num: 110290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*935G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1026G>A
  hgvsp: ENST00000278224.9:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.589G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3284G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*844G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1275G>A
  hgvsp: ENST00000380525.4:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.996G>A
  hgvsp: ENST00000397114.3:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1026G>A
  hgvsp: ENST00000397111.5:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1065G>A
  hgvsp: ENST00000401769.3:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro425Pro
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-3040490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040490
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040490
    reference: chr 11
allele count: 1
allele frequency: 9.087439341342396e-6
allele num: 110042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1025C>T
  hgvsp: ENSP00000380300.5:p.Pro342Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.995C>T
  hgvsp: ENSP00000380303.3:p.Pro332Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1025C>T
  hgvsp: ENSP00000278224.9:p.Pro342Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3283C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1064C>T
  hgvsp: ENSP00000384069.3:p.Pro355Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.588C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*843C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1274C>T
  hgvsp: ENSP00000369897.4:p.Pro425Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*934C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro425Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

11-3040493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040493
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040493
    reference: chr 11
allele count: 4
allele frequency: 3.636165300074542e-5
allele num: 110006
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1271G>A
  hgvsp: ENSP00000369897.4:p.Arg424His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*931G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.585G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1022G>A
  hgvsp: ENSP00000380300.5:p.Arg341His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.992G>A
  hgvsp: ENSP00000380303.3:p.Arg331His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3280G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1061G>A
  hgvsp: ENSP00000384069.3:p.Arg354His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1022G>A
  hgvsp: ENSP00000278224.9:p.Arg341His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*840G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg424His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

11-3040510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040510
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040510
    reference: chr 11
allele count: 5
allele frequency: 4.578083797245825e-5
allele num: 109216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-13C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-13C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3565
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/11-3040516-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040516
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040516
    reference: chr 11
allele count: 1
allele frequency: 9.1746486109582e-6
allele num: 108996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-19T>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-19T>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS

http://identifiers.org/exac.variant/11-3040532-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040532
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040532
    reference: chr 11
allele count: 1
allele frequency: 9.22969006700755e-6
allele num: 108346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-35G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-35G>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

11-3040537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040537
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040537
    reference: chr 11
allele count: 24
allele frequency: 2.219304248118215e-4
allele num: 108142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-40G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-40G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-3040540-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040540
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040540
    reference: chr 11
allele count: 2
allele frequency: 1.85106343594395e-5
allele num: 108046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-43A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-43A>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

11-3040542-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040542
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040542
    reference: chr 11
allele count: 3
allele frequency: 2.779630865021125e-5
allele num: 107928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-45C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-45C>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

11-3040545-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040545
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040545
    reference: chr 11
allele count: 1
allele frequency: 9.273169012778427e-6
allele num: 107838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-48G>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1271
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-3040549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3040549
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3040549
    reference: chr 11
allele count: 36
allele frequency: 3.341067285382831e-4
allele num: 107750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1018-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1267-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.988-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*836-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1057-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*927-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3276-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.581-52G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1018-52G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

11-3041402-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041402
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041402
    reference: chr 11
allele count: 162
allele frequency: 1.403034712118063e-3
allele num: 115464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+48G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+48G>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13097
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9802
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24900
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 3.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum

11-3041403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041403
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041403
    reference: chr 11
allele count: 4
allele frequency: 3.341240936883959e-5
allele num: 119716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+47C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+47C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-3041410-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041410
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041410
    reference: chr 11
allele count: 1
allele frequency: 8.341396683460679e-6
allele num: 119884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+40G>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+40G>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35973
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ

11-3041416-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041416
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041416
    reference: chr 11
allele count: 2
allele frequency: 1.663838141825563e-5
allele num: 120204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+34A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+34A>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

11-3041424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041424
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041424
    reference: chr 11
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+26G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+26G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-3041429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041429
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041429
    reference: chr 11
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+21G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+21G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-3041438-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041438
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041438
    reference: chr 11
allele count: 2
allele frequency: 1.655382476121108e-5
allele num: 120818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+12G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+12G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2965
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum

11-3041443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041443
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041443
    reference: chr 11
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+7G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+7G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12992
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10559
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1266+7G>A
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

11-3041444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041444
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041444
    reference: chr 11
allele count: 2291
allele frequency: 1.89367013274702e-2
allele num: 120982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.987+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*926+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.580+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1056+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*835+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1017+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1017+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3275+6C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1266+6C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13441
  bin: 3.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.25e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12688
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 734
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 27033
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 3.75e1
  variant carriers: 74
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38468
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1266+6C>T
num of homozygotes: 252
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

11-3041460-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041460
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041460
    reference: chr 11
allele count: 4
allele frequency: 3.301474108189306e-5
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*825C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1256C>G
  hgvsp: ENSP00000369897.4:p.Pro419Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1046C>G
  hgvsp: ENSP00000384069.3:p.Pro349Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*916C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3265C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1007C>G
  hgvsp: ENSP00000380300.5:p.Pro336Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1007C>G
  hgvsp: ENSP00000278224.9:p.Pro336Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.977C>G
  hgvsp: ENSP00000380303.3:p.Pro326Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.570C>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12944
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro419Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-3041465-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041465
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041465
    reference: chr 11
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3260G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.972G>A
  hgvsp: ENST00000397114.3:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1251G>A
  hgvsp: ENST00000380525.4:c.1251G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*911G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1002G>A
  hgvsp: ENST00000397111.5:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1041G>A
  hgvsp: ENST00000401769.3:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1002G>A
  hgvsp: ENST00000278224.9:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.565G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*820G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10780
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro417Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

11-3041466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041466
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041466
    reference: chr 11
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1250C>T
  hgvsp: ENSP00000369897.4:p.Pro417Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.971C>T
  hgvsp: ENSP00000380303.3:p.Pro324Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3259C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*819C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*910C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.1001C>T
  hgvsp: ENSP00000380300.5:p.Pro334Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.1001C>T
  hgvsp: ENSP00000278224.9:p.Pro334Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1040C>T
  hgvsp: ENSP00000384069.3:p.Pro347Leu
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.564C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro417Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-3041474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041474
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041474
    reference: chr 11
allele count: 31
allele frequency: 2.55729158073617e-4
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*902G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.556G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1242G>A
  hgvsp: ENST00000380525.4:c.1242G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.993G>A
  hgvsp: ENST00000278224.9:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.963G>A
  hgvsp: ENST00000397114.3:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1032G>A
  hgvsp: ENST00000401769.3:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.993G>A
  hgvsp: ENST00000397111.5:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3251G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*811G>A
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13903
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro414Pro
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

11-3041476-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041476
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041476
    reference: chr 11
allele count: 2
allele frequency: 1.649647800194658e-5
allele num: 121238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*809C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1030C>G
  hgvsp: ENSP00000384069.3:p.Pro344Ala
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.961C>G
  hgvsp: ENSP00000380303.3:p.Pro321Ala
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.991C>G
  hgvsp: ENSP00000380300.5:p.Pro331Ala
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3249C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1240C>G
  hgvsp: ENSP00000369897.4:p.Pro414Ala
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.991C>G
  hgvsp: ENSP00000278224.9:p.Pro331Ala
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.554C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*900C>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro414Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

11-3041482-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041482
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041482
    reference: chr 11
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1234G>A
  hgvsp: ENSP00000369897.4:p.Gly412Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.955G>A
  hgvsp: ENSP00000380303.3:p.Gly319Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.985G>A
  hgvsp: ENSP00000380300.5:p.Gly329Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*803G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1024G>A
  hgvsp: ENSP00000384069.3:p.Gly342Arg
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*894G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.548G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3243G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.985G>A
  hgvsp: ENSP00000278224.9:p.Gly329Arg
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly412Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

11-3041483-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041483
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041483
    reference: chr 11
allele count: 5
allele frequency: 4.123031252576895e-5
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*893C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*802C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.954C>T
  hgvsp: ENST00000397114.3:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1023C>T
  hgvsp: ENST00000401769.3:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.547C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.984C>T
  hgvsp: ENST00000278224.9:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.984C>T
  hgvsp: ENST00000397111.5:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3242C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1233C>T
  hgvsp: ENST00000380525.4:c.1233C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro411Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

11-3041491-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041491
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041491
    reference: chr 11
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.539T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.976T>C
  hgvsp: ENSP00000380300.5:p.Ser326Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1225T>C
  hgvsp: ENSP00000369897.4:p.Ser409Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*794T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.976T>C
  hgvsp: ENSP00000278224.9:p.Ser326Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*885T>C
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1015T>C
  hgvsp: ENSP00000384069.3:p.Ser339Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.946T>C
  hgvsp: ENSP00000380303.3:p.Ser316Pro
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3234T>C
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2482
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser409Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

11-3041494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041494
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041494
    reference: chr 11
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.943G>A
  hgvsp: ENSP00000380303.3:p.Ala315Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3231G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*791G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.536G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*882G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.973G>A
  hgvsp: ENSP00000278224.9:p.Ala325Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.973G>A
  hgvsp: ENSP00000380300.5:p.Ala325Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1012G>A
  hgvsp: ENSP00000384069.3:p.Ala338Thr
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1222G>A
  hgvsp: ENSP00000369897.4:p.Ala408Thr
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala408Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/11-3041506-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041506
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041506
    reference: chr 11
allele count: 19
allele frequency: 1.566286910787595e-4
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.961G>T
  hgvsp: ENSP00000380300.5:p.Ala321Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.524G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.961G>T
  hgvsp: ENSP00000278224.9:p.Ala321Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*779G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1210G>T
  hgvsp: ENSP00000369897.4:p.Ala404Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.1000G>T
  hgvsp: ENSP00000384069.3:p.Ala334Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.931G>T
  hgvsp: ENSP00000380303.3:p.Ala311Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*870G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3219G>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala404Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

11-3041513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041513
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041513
    reference: chr 11
allele count: 18
allele frequency: 1.48404650012367e-4
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*863C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.954C>T
  hgvsp: ENST00000397111.5:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.954C>T
  hgvsp: ENST00000278224.9:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*772C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.924C>T
  hgvsp: ENST00000397114.3:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.993C>T
  hgvsp: ENST00000401769.3:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.517C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1203C>T
  hgvsp: ENST00000380525.4:c.1203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3212C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12927
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn401Asn
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

11-3041514-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041514
    reference: chr 11
allele count: 21
allele frequency: 1.731416133500429e-4
allele num: 121288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.516A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1202A>G
  hgvsp: ENSP00000369897.4:p.Asn401Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*862A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.953A>G
  hgvsp: ENSP00000278224.9:p.Asn318Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.953A>G
  hgvsp: ENSP00000380300.5:p.Asn318Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.992A>G
  hgvsp: ENSP00000384069.3:p.Asn331Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.923A>G
  hgvsp: ENSP00000380303.3:p.Asn308Ser
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3211A>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*771A>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39920
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn401Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

11-3041516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041516
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041516
    reference: chr 11
allele count: 7
allele frequency: 5.771862992463596e-5
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.921C>T
  hgvsp: ENST00000397114.3:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.951C>T
  hgvsp: ENST00000278224.9:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.990C>T
  hgvsp: ENST00000401769.3:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1200C>T
  hgvsp: ENST00000380525.4:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.951C>T
  hgvsp: ENST00000397111.5:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.514C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*769C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*860C>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3209C>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro400Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

11-3041520-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041520
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041520
    reference: chr 11
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.986C>G
  hgvsp: ENSP00000384069.3:p.Ser329Cys
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.947C>G
  hgvsp: ENSP00000278224.9:p.Ser316Cys
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1196C>G
  hgvsp: ENSP00000369897.4:p.Ser399Cys
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.947C>G
  hgvsp: ENSP00000380300.5:p.Ser316Cys
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.510C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.917C>G
  hgvsp: ENSP00000380303.3:p.Ser306Cys
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3205C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*765C>G
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*856C>G
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser399Cys
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-3041525-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041525
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041525
    reference: chr 11
allele count: 16
allele frequency: 1.319783555496899e-4
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*851G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.942G>T
  hgvsp: ENSP00000380300.5:p.Lys314Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.912G>T
  hgvsp: ENSP00000380303.3:p.Lys304Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*760G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.942G>T
  hgvsp: ENSP00000278224.9:p.Lys314Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.981G>T
  hgvsp: ENSP00000384069.3:p.Lys327Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1191G>T
  hgvsp: ENSP00000369897.4:p.Lys397Asn
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3200G>T
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.505G>T
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13923
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28143
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys397Asn
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-3041538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3041538
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3041538
    reference: chr 11
allele count: 10
allele frequency: 8.260639703938673e-5
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000465240
  gene symbol: CARS
  hgvsc: ENST00000465240.1:n.492G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000431368
  ensembl transcript: ENST00000531387
  gene symbol: CARS
  hgvsc: ENST00000531387.1:c.*838G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000278224
  ensembl transcript: ENST00000278224
  gene symbol: CARS
  hgvsc: ENST00000278224.9:c.929G>A
  hgvsp: ENSP00000278224.9:p.Arg310His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380303
  ensembl transcript: ENST00000397114
  gene symbol: CARS
  hgvsc: ENST00000397114.3:c.899G>A
  hgvsp: ENSP00000380303.3:p.Arg300His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000384069
  ensembl transcript: ENST00000401769
  gene symbol: CARS
  hgvsc: ENST00000401769.3:c.968G>A
  hgvsp: ENSP00000384069.3:p.Arg323His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000432619
  ensembl transcript: ENST00000529772
  gene symbol: CARS
  hgvsc: ENST00000529772.1:c.*747G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000380300
  ensembl transcript: ENST00000397111
  gene symbol: CARS
  hgvsc: ENST00000397111.5:c.929G>A
  hgvsp: ENSP00000380300.5:p.Arg310His
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110619
  ensembl transcript: ENST00000526890
  gene symbol: CARS
  hgvsc: ENST00000526890.1:n.3187G>A
  variant of: http://identifiers.org/hgnc/1493
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110619
  ensembl protein: ENSP00000369897
  ensembl transcript: ENST00000380525
  gene symbol: CARS
  hgvsc: ENST00000380525.4:c.1178G>A
  hgvsp: ENSP00000369897.4:p.Arg393His
  variant of: http://identifiers.org/hgnc/1493
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg393His
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47291
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63970
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.56712519589065e-3
allele num: 11486
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: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e0

QD
type: SiteQuality
SIO_000300: 1.312e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

FS
type: SiteQuality
SIO_000300: 5.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

DP
type: SiteQuality
SIO_000300: 3.680276e6

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
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: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9366
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.208e0

DP
type: SiteQuality
SIO_000300: 3.682558e6

FS
type: SiteQuality
SIO_000300: 6.07e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 9.76e0

GenotypeQuality
all individuals: 2776
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3400
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 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: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562695336917115e-5
allele num: 63992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.198e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

FS
type: SiteQuality
SIO_000300: 1.758e0

DP
type: SiteQuality
SIO_000300: 3.683362e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.412e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

GenotypeQuality
all individuals: 715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562646498109198e-5
allele num: 63994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9396
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: 11486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.06e-1

FS
type: SiteQuality
SIO_000300: 5.291e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.562e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

QD
type: SiteQuality
SIO_000300: 1.076e1

DP
type: SiteQuality
SIO_000300: 3.683339e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

GenotypeQuality
all individuals: 461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 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: 1
allele frequency: 1.168770453482936e-4
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.683676e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: -3.99e-1

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3470
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
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: 10222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561816705191479e-5
allele num: 64028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.205e-1

DP
type: SiteQuality
SIO_000300: 3.685856e6

QD
type: SiteQuality
SIO_000300: 1.323e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

GenotypeQuality
all individuals: 688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3534
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64068
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: 1
allele frequency: 1.259445843828715e-3
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 3.688554e6

QD
type: SiteQuality
SIO_000300: 1.129e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3534
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
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: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64068
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.168497312456181e-3
allele num: 8558
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.126954346466542e-4
allele num: 9594
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 3.688554e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

GenotypeQuality
all individuals: 3379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47288
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560598021161709e-5
allele num: 64078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
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: 11492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.986e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

DP
type: SiteQuality
SIO_000300: 3.687139e6

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 2.725e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.97e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

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

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 960
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560208443848098e-5
allele num: 64094
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: 10224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 3.687696e6

FS
type: SiteQuality
SIO_000300: 3.268e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.051e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.45e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeQuality
all individuals: 261
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3587
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
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: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64092
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.451e0

QD
type: SiteQuality
SIO_000300: 1.341e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.666e0

MQRankSum
type: SiteQuality
SIO_000300: 8.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 3.688049e6

MQ
type: SiteQuality
SIO_000300: 5.989e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.24e-1

GenotypeQuality
all individuals: 464
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
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: 64122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.930832356389214e-4
allele num: 10236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.76e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 2.339e0

QD
type: SiteQuality
SIO_000300: 1.441e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 3.688857e6

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47286
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 170
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558797855094152e-5
allele num: 64152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 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: 8570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.943e0

FS
type: SiteQuality
SIO_000300: 1.801e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

DP
type: SiteQuality
SIO_000300: 3.689409e6

QD
type: SiteQuality
SIO_000300: 1.23e1

GenotypeQuality
all individuals: 328
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.25e1
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: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558943659776136e-5
allele num: 64146
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.688984e6

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 2.481e0

VQSLOD
type: SiteQuality
SIO_000300: -4.816e-1

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 187
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47286
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
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: 1
allele frequency: 1.007252215954875e-4
allele num: 9928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.688973e6

FS
type: SiteQuality
SIO_000300: 6.113e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.001e0

VQSLOD
type: SiteQuality
SIO_000300: -2.306e0

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

QD
type: SiteQuality
SIO_000300: 6.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.226e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47289
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 461
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.173249902229175e-3
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559089491736826e-5
allele num: 64140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
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: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.688766e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.561e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

GenotypeQuality
all individuals: 3527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3678
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.777082518576456e-5
allele num: 10228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
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
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allele frequency: 0.0e0
allele num: 64138
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.687597e6

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

QD
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
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SIO_000300: -1.057e0

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: 5.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.559040878051823e-5
allele num: 64142
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
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allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.992e1

VQSLOD
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SIO_000300: 2.5e-2

MQRankSum
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SIO_000300: -7.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.233e0

QD
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SIO_000300: 1.322e1

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

East Asian
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allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 9.893153937475267e-5
allele num: 10108
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.558846453624318e-5
allele num: 64150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.104e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 1.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 9.581e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.437e0

DP
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SIO_000300: 3.687457e6

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

South Asian
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allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

European (Finnish)
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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: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64160
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

VQSLOD
type: SiteQuality
SIO_000300: -5.871e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.916e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.636e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.879e0

DP
type: SiteQuality
SIO_000300: 3.686995e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64172
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.611e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.687217e6

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
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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African
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allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.238303181534623e-5
allele num: 64120
num of homozygotes: 0

Other
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MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

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

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

Other
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allele num: 806
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64082
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African
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Latino
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South Asian
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allele num: 10214
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MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 10214
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African
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Latino
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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allele count: 30
allele frequency: 4.681501825785712e-4
allele num: 64082
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64066
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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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Latino
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South Asian
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allele num: 10212
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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DP
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.904e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
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: 64012
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.674414e6

MQRankSum
type: SiteQuality
SIO_000300: -9.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 3.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.552e0

VQSLOD
type: SiteQuality
SIO_000300: -1.301e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.092e0

QD
type: SiteQuality
SIO_000300: 1.616e1

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.742160278745645e-4
allele num: 11480
num of homozygotes: 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: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.688965301656768e-5
allele num: 63980
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.263e1

DP
type: SiteQuality
SIO_000300: 3.673592e6

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 867
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GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.821253191907288e-5
allele num: 10182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63962
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.445e1

FS
type: SiteQuality
SIO_000300: 1.1949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 3.672364e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.365e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 128
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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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bin: 9.75e1
variant carriers: 7

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: 861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63944
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.215962441314554e-4
allele num: 8520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.763e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

DP
type: SiteQuality
SIO_000300: 3.671711e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.394e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

GenotypeQuality
all individuals: 3771
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
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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
all individuals: 679
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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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 456
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566072603125881e-5
allele num: 63854
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.919e0

DP
type: SiteQuality
SIO_000300: 3.666341e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.082e0

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeQuality
all individuals: 678
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
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GenotypeQuality
all individuals: 811
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 56
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 121
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variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63848
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.906875371507826e-5
allele num: 10094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.99e-1

DP
type: SiteQuality
SIO_000300: 3.666192e6

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.36e0

FS
type: SiteQuality
SIO_000300: 6.209e0

QD
type: SiteQuality
SIO_000300: 1.338e1

GenotypeQuality
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bin: 1.75e1
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: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.724480893386844e-5
allele num: 11462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567496394758292e-5
allele num: 63796
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 2.631e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.29e1

DP
type: SiteQuality
SIO_000300: 3.662963e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 625
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.729050279329609e-5
allele num: 11456
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63792
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.289e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.234e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 4.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 3.661792e6

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
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GenotypeQuality
all individuals: 172
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 37
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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: 3.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.28002637611078e-5
allele num: 63694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9930
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.65779e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: 9.330000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.756e0

QD
type: SiteQuality
SIO_000300: 1.198e1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.175e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.727834336684843e-5
allele num: 63454
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 1.057e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.71e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

FS
type: SiteQuality
SIO_000300: 5.101e0

DP
type: SiteQuality
SIO_000300: 3.645469e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 605
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variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.577884372633173e-5
allele num: 63376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.628e0

DP
type: SiteQuality
SIO_000300: 3.641415e6

MQ
type: SiteQuality
SIO_000300: 5.935e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 5.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 252
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variant carriers: 0

GenotypeQuality
all individuals: 47250
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.544077552256892e-4
allele num: 6602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578332649389185e-5
allele num: 63358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.640666e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 1.159e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.172e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 454
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2079
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 318
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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: 944
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.758128469468675e-5
allele num: 63050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.755001755001755e-4
allele num: 11396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.626336e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

FS
type: SiteQuality
SIO_000300: 2.712e0

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

QD
type: SiteQuality
SIO_000300: 1.174e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 1933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 209
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GenotypeQuality
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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
all individuals: 259
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variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589218740067383e-5
allele num: 62924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.313e1

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

DP
type: SiteQuality
SIO_000300: 3.619823e6

FS
type: SiteQuality
SIO_000300: 1.859e0

GenotypeQuality
all individuals: 1581
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 518
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598312182335454e-5
allele num: 62566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

DP
type: SiteQuality
SIO_000300: 3.607696e6

FS
type: SiteQuality
SIO_000300: 6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.61e0

QD
type: SiteQuality
SIO_000300: 1.613e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 459
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 145
bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 23

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62428
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: 24
allele frequency: 2.685164466323563e-3
allele num: 8938
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.81e0

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

QD
type: SiteQuality
SIO_000300: 1.375e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.783e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.604743e6

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 198
bin: 4.75e1
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GenotypeQuality
all individuals: 404
bin: 2.75e1
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GenotypeQuality
all individuals: 326
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 649
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62362
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.034126163391934e-4
allele num: 9670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.247e1

MQ
type: SiteQuality
SIO_000300: 5.907e1

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

DP
type: SiteQuality
SIO_000300: 3.602214e6

VQSLOD
type: SiteQuality
SIO_000300: -5.679e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 2.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeQuality
all individuals: 47240
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 3.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.798169980644026e-5
allele num: 11366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.210891343436938e-5
allele num: 62288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8932
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

FS
type: SiteQuality
SIO_000300: 2.534e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 2.385e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

VQSLOD
type: SiteQuality
SIO_000300: -1.377e0

DP
type: SiteQuality
SIO_000300: 3.601522e6

GenotypeQuality
all individuals: 398
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 547
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variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.606890345802802e-5
allele num: 62232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 9.329000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.594e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 3.600782e6

GenotypeQuality
all individuals: 1190
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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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variant carriers: 36

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608078988839932e-5
allele num: 62186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.76242509693338e-4
allele num: 11348
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 3.441084462982273e-3
allele num: 9590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 3.611e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.072e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

DP
type: SiteQuality
SIO_000300: 3.600334e6

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
all individuals: 576
bin: 5.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2303
bin: 7.25e1
variant carriers: 3

GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 247
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 7

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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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 65

GenotypeQuality
all individuals: 381
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GenotypeQuality
all individuals: 1234
bin: 4.75e1
variant carriers: 8

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.748906386701662e-5
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.222493887530562e-3
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.075471698113207e-4
allele num: 8480
num of homozygotes: 0

African
type: Population
allele count: 54
allele frequency: 5.668696199874029e-3
allele num: 9526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 79
allele frequency: 1.246607334469482e-3
allele num: 63372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 21
allele frequency: 3.643303261623872e-3
allele num: 5764
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e0

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

QD
type: SiteQuality
SIO_000300: 2.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.153e0

VQSLOD
type: SiteQuality
SIO_000300: -7.697e0

DP
type: SiteQuality
SIO_000300: 1.696097e6

MQ
type: SiteQuality
SIO_000300: 5.895e1

FS
type: SiteQuality
SIO_000300: 2.9391e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.608e0

GenotypeQuality
all individuals: 710
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1003
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GenotypeQuality
all individuals: 1026
bin: 3.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.467406380027739e-4
allele num: 11536
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.439e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

FS
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

DP
type: SiteQuality
SIO_000300: 1.690138e6

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
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: 11544
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518787400139728e-5
allele num: 65842
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.704071e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 9.52e0

FS
type: SiteQuality
SIO_000300: 3.105e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.030762236702531e-5
allele num: 65990
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.433e0

DP
type: SiteQuality
SIO_000300: 1.716063e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 201
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66172
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.515e0

MQRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.728811e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 9.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

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

GenotypeQuality
all individuals: 38238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10452
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 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: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.879e0

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

DP
type: SiteQuality
SIO_000300: 1.733359e6

QD
type: SiteQuality
SIO_000300: 1.141e1

GenotypeQuality
all individuals: 2466
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38552
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 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: 2
allele frequency: 3.014408874419726e-5
allele num: 66348
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.078e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

FS
type: SiteQuality
SIO_000300: 1.305e0

VQSLOD
type: SiteQuality
SIO_000300: 4.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.739556e6

QD
type: SiteQuality
SIO_000300: 1.254e1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

GenotypeQuality
all individuals: 271
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38724
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2640
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2488
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.901e0

FS
type: SiteQuality
SIO_000300: 2.682e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -2.006e0

QD
type: SiteQuality
SIO_000300: 2.024e1

DP
type: SiteQuality
SIO_000300: 1.741751e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 7.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2552
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1292
bin: 8.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 605
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3934
bin: 9.75e1
variant carriers: 2024

GenotypeQuality
all individuals: 10407
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 6.624111766831266e-4
allele num: 66424
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

Latino
type: Population
allele count: 104
allele frequency: 8.991872730416739e-3
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.530973451327434e-3
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 2136
allele frequency: 2.058596761757903e-1
allele num: 10376
num of homozygotes: 252

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.554e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

FS
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.834e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.01e0

DP
type: SiteQuality
SIO_000300: 1.831048e6

GenotypeQuality
all individuals: 2488
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10774
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39792
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005530175522962e-5
allele num: 66544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.735911e6

FS
type: SiteQuality
SIO_000300: 1.831e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.252e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39772
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.736174e6

QD
type: SiteQuality
SIO_000300: 8.51e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.166e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.203e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.424e0

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

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10793
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 8.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

DP
type: SiteQuality
SIO_000300: 1.73626e6

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2647
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2156
bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 10795
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39865
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.753866482476951e-4
allele num: 66598
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

FS
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

QD
type: SiteQuality
SIO_000300: 1.03e1

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

DP
type: SiteQuality
SIO_000300: 1.738693e6

BaseQRankSum
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SIO_000300: -9.47e-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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African
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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QD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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FS
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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Other
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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MQRankSum
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VQSLOD
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FS
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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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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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Other
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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East Asian
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Latino
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Other
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European (Non-Finnish)
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InbreedingCoeff
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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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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South Asian
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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DP
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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Other
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South Asian
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10802
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
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: 6594
num of homozygotes: 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: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.094357076780758e-4
allele num: 8648
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 2.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.905e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.034e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 1.736697e6

MQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

GenotypeQuality
all individuals: 10801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39918
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2083
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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)
type: Population
allele count: 1
allele frequency: 1.517450682852807e-4
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.153e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.735796e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.09e-1

QD
type: SiteQuality
SIO_000300: 4.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.917e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 2641
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39884
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 1345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10799
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.401825387294344e-4
allele num: 66616
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.735766e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.638e0

QD
type: SiteQuality
SIO_000300: 1.114e1

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

FS
type: SiteQuality
SIO_000300: 2.887e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 10744
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0