3-140675422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675422
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675422
    reference: chr 3
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.297C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.95C>T
  hgvsp: ENSP00000391521.2:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-56C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-56C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.95C>T
  hgvsp: ENSP00000421470.1:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.95C>T
  hgvsp: ENSP00000320688.6:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.282C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.95C>T
  hgvsp: ENSP00000423319.1:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.95C>T
  hgvsp: ENSP00000401938.2:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.307C>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10922
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2935
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr32Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

3-140675424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675424
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675424
    reference: chr 3
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.97C>T
  hgvsp: ENSP00000423319.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.284C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.97C>T
  hgvsp: ENSP00000421470.1:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.97C>T
  hgvsp: ENSP00000320688.6:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.309C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.97C>T
  hgvsp: ENSP00000391521.2:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.299C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.97C>T
  hgvsp: ENSP00000401938.2:p.Arg33Ter
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg33Ter
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

3-140675427-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675427
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675427
    reference: chr 3
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.312C>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.100C>G
  hgvsp: ENSP00000401938.2:p.Leu34Val
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.100C>G
  hgvsp: ENSP00000421470.1:p.Leu34Val
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.287C>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.100C>G
  hgvsp: ENSP00000423319.1:p.Leu34Val
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.302C>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.100C>G
  hgvsp: ENSP00000320688.6:p.Leu34Val
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.100C>G
  hgvsp: ENSP00000391521.2:p.Leu34Val
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-51C>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-51C>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu34Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/3-140675435-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675435
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675435
    reference: chr 3
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-43A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.310A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.108A>C
  hgvsp: ENST00000324194.6:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.295A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.108A>C
  hgvsp: ENST00000507429.1:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.108A>C
  hgvsp: ENST00000502594.1:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-43A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.108A>C
  hgvsp: ENST00000453248.2:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.108A>C
  hgvsp: ENST00000446041.2:c.108A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.320A>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3672
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser36Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-140675435-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675435
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675432
    reference: chr 3
allele count: 44
allele frequency: 3.626174386022746e-4
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.112_114delTCT
  hgvsp: ENSP00000320688.6:p.Ser38del
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.314_316delTCT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-39_-37delTCT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.112_114delTCT
  hgvsp: ENSP00000423319.1:p.Ser38del
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.112_114delTCT
  hgvsp: ENSP00000421470.1:p.Ser38del
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.299_301delTCT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.112_114delTCT
  hgvsp: ENSP00000401938.2:p.Ser38del
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.324_326delTCT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.112_114delTCT
  hgvsp: ENSP00000391521.2:p.Ser38del
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-39_-37delTCT
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 11510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser38del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: ATCT
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

3-140675447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675447
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675447
    reference: chr 3
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.307G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.120G>A
  hgvsp: ENST00000324194.6:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.120G>A
  hgvsp: ENST00000507429.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.120G>A
  hgvsp: ENST00000502594.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.120G>A
  hgvsp: ENST00000446041.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.120G>A
  hgvsp: ENST00000453248.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.322G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.332G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr40Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

3-140675451-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675451
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675451
    reference: chr 3
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.124T>C
  hgvsp: ENSP00000391521.2:p.Tyr42His
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.311T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.326T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.124T>C
  hgvsp: ENSP00000401938.2:p.Tyr42His
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.124T>C
  hgvsp: ENSP00000421470.1:p.Tyr42His
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.124T>C
  hgvsp: ENSP00000423319.1:p.Tyr42His
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.124T>C
  hgvsp: ENSP00000320688.6:p.Tyr42His
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.336T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr42His
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

3-140675452-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675452
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675452
    reference: chr 3
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.337A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-26A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.327A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.125A>G
  hgvsp: ENSP00000320688.6:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.125A>G
  hgvsp: ENSP00000423319.1:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.125A>G
  hgvsp: ENSP00000401938.2:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.125A>G
  hgvsp: ENSP00000391521.2:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.312A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-26A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.125A>G
  hgvsp: ENSP00000421470.1:p.Tyr42Cys
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29061
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr42Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-140675469-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675469
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675469
    reference: chr 3
allele count: 261
allele frequency: 2.150980715345311e-3
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.142C>T
  hgvsp: ENST00000453248.2:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.344C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.142C>T
  hgvsp: ENST00000507429.1:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.329C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.142C>T
  hgvsp: ENST00000324194.6:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.142C>T
  hgvsp: ENST00000502594.1:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.354C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.142C>T
  hgvsp: ENST00000446041.2:c.142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11459
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu48Leu
num of homozygotes: 5
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

3-140675490-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675490
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675490
    reference: chr 3
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.350A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.13A>G
  hgvsp: ENSP00000424505.1:p.Ser5Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.163A>G
  hgvsp: ENSP00000423319.1:p.Ser55Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.163A>G
  hgvsp: ENSP00000320688.6:p.Ser55Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.163A>G
  hgvsp: ENSP00000421470.1:p.Ser55Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.375A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.13A>G
  hgvsp: ENSP00000422265.1:p.Ser5Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.365A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.13A>G
  hgvsp: ENSP00000423711.1:p.Ser5Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.163A>G
  hgvsp: ENSP00000391521.2:p.Ser55Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.163A>G
  hgvsp: ENSP00000401938.2:p.Ser55Gly
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser55Gly
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

3-140675492-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675492
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675492
    reference: chr 3
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.165T>A
  hgvsp: ENSP00000320688.6:p.Ser55Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.15T>A
  hgvsp: ENSP00000423711.1:p.Ser5Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.165T>A
  hgvsp: ENSP00000423319.1:p.Ser55Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.15T>A
  hgvsp: ENSP00000422265.1:p.Ser5Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.165T>A
  hgvsp: ENSP00000401938.2:p.Ser55Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.165T>A
  hgvsp: ENSP00000421470.1:p.Ser55Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.377T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.352T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.15T>A
  hgvsp: ENSP00000424505.1:p.Ser5Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.165T>A
  hgvsp: ENSP00000391521.2:p.Ser55Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.367T>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser55Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-140675498-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675498
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675498
    reference: chr 3
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.171C>A
  hgvsp: ENSP00000391521.2:p.Asn57Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.21C>A
  hgvsp: ENSP00000423711.1:p.Asn7Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.21C>A
  hgvsp: ENSP00000424505.1:p.Asn7Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.383C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.171C>A
  hgvsp: ENSP00000401938.2:p.Asn57Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.171C>A
  hgvsp: ENSP00000320688.6:p.Asn57Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.373C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.171C>A
  hgvsp: ENSP00000421470.1:p.Asn57Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.358C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.21C>A
  hgvsp: ENSP00000422265.1:p.Asn7Lys
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.171C>A
  hgvsp: ENSP00000423319.1:p.Asn57Lys
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn57Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-140675499-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675499
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675499
    reference: chr 3
allele count: 2
allele frequency: 1.650764303872693e-5
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.359C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.172C>A
  hgvsp: ENST00000446041.2:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.172C>A
  hgvsp: ENST00000507429.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.22C>A
  hgvsp: ENST00000512023.1:c.22C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.172C>A
  hgvsp: ENST00000502594.1:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.22C>A
  hgvsp: ENST00000512506.1:c.22C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.384C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.172C>A
  hgvsp: ENST00000324194.6:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.374C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.172C>A
  hgvsp: ENST00000453248.2:c.172C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.22C>A
  hgvsp: ENST00000513887.1:c.22C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg58Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

3-140675500-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675500
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675500
    reference: chr 3
allele count: 6
allele frequency: 4.952374663651221e-5
allele num: 121154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.173G>A
  hgvsp: ENSP00000423319.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.360G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.173G>A
  hgvsp: ENSP00000320688.6:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.23G>A
  hgvsp: ENSP00000423711.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.23G>A
  hgvsp: ENSP00000422265.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.173G>A
  hgvsp: ENSP00000401938.2:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.173G>A
  hgvsp: ENSP00000421470.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.385G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.23G>A
  hgvsp: ENSP00000424505.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.173G>A
  hgvsp: ENSP00000391521.2:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.375G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg58Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

3-140675506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675506
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675506
    reference: chr 3
allele count: 148
allele frequency: 1.222857520573752e-3
allele num: 121028
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.179T>C
  hgvsp: ENSP00000320688.6:p.Val60Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.29T>C
  hgvsp: ENSP00000424505.1:p.Val10Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.381T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.179T>C
  hgvsp: ENSP00000401938.2:p.Val60Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.29T>C
  hgvsp: ENSP00000423711.1:p.Val10Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.179T>C
  hgvsp: ENSP00000421470.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.29T>C
  hgvsp: ENSP00000422265.1:p.Val10Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.179T>C
  hgvsp: ENSP00000423319.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.366T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.179T>C
  hgvsp: ENSP00000391521.2:p.Val60Ala
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.391T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 12358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val60Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-140675507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675507
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675507
    reference: chr 3
allele count: 7
allele frequency: 5.784454691192755e-5
allele num: 121014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.180G>A
  hgvsp: ENST00000453248.2:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.180G>A
  hgvsp: ENST00000446041.2:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.180G>A
  hgvsp: ENST00000324194.6:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.180G>A
  hgvsp: ENST00000502594.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.180G>A
  hgvsp: ENST00000507429.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.30G>A
  hgvsp: ENST00000512506.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.392G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.30G>A
  hgvsp: ENST00000513887.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.382G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.30G>A
  hgvsp: ENST00000512023.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.367G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12368
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val60Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

3-140675513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675513
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675513
    reference: chr 3
allele count: 1
allele frequency: 8.276227364518158e-6
allele num: 120828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.186C>T
  hgvsp: ENST00000446041.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.36C>T
  hgvsp: ENST00000512023.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.373C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.398C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.186C>T
  hgvsp: ENST00000507429.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.186C>T
  hgvsp: ENST00000502594.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.186C>T
  hgvsp: ENST00000453248.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.186C>T
  hgvsp: ENST00000324194.6:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.36C>T
  hgvsp: ENST00000513887.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.36C>T
  hgvsp: ENST00000512506.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.388C>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro62Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-140675514-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675514
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675514
    reference: chr 3
allele count: 6
allele frequency: 4.966229638458482e-5
allele num: 120816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.399G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.187G>A
  hgvsp: ENSP00000320688.6:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.37G>A
  hgvsp: ENSP00000422265.1:p.Gly13Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.37G>A
  hgvsp: ENSP00000423711.1:p.Gly13Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.389G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.187G>A
  hgvsp: ENSP00000423319.1:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.187G>A
  hgvsp: ENSP00000391521.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.187G>A
  hgvsp: ENSP00000421470.1:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.187G>A
  hgvsp: ENSP00000401938.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.374G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.37G>A
  hgvsp: ENSP00000424505.1:p.Gly13Arg
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11405
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly63Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

3-140675531-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675531
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675531
    reference: chr 3
allele count: 4
allele frequency: 3.32695666638942e-5
allele num: 120230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.204A>G
  hgvsp: ENST00000507429.1:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.204A>G
  hgvsp: ENST00000446041.2:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.416A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.204A>G
  hgvsp: ENST00000324194.6:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.406A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.54A>G
  hgvsp: ENST00000512023.1:c.54A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.204A>G
  hgvsp: ENST00000453248.2:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.54A>G
  hgvsp: ENST00000512506.1:c.54A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.204A>G
  hgvsp: ENST00000502594.1:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.391A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.54A>G
  hgvsp: ENST00000513887.1:c.54A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11361
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16202
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.204A>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

3-140675555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675555
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675555
    reference: chr 3
allele count: 2
allele frequency: 1.682878395207162e-5
allele num: 118844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.440G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+22G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+22G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

3-140675556-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675556
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675556
    reference: chr 3
allele count: 2
allele frequency: 1.682708487581611e-5
allele num: 118856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.441T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+23T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+23T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3608
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

3-140675560-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675560
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675560
    reference: chr 3
allele count: 1
allele frequency: 8.437394532568342e-6
allele num: 118520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.445T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+27T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+27T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum

3-140675563-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675563
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675563
    reference: chr 3
allele count: 1
allele frequency: 8.444804756114038e-6
allele num: 118416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.448T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+30T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+30T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

3-140675568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675568
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675568
    reference: chr 3
allele count: 1
allele frequency: 8.472996559963397e-6
allele num: 118022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.453T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+35T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+35T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

3-140675569-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675569
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675569
    reference: chr 3
allele count: 1
allele frequency: 8.498342823149486e-6
allele num: 117670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.454G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+36G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+36G>T
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

3-140675570-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675570
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675570
    reference: chr 3
allele count: 1
allele frequency: 8.499643014993371e-6
allele num: 117652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.455T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+37T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+37T>G
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

3-140675574-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675574
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675574
    reference: chr 3
allele count: 1
allele frequency: 8.533588203167667e-6
allele num: 117184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.459C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+41C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+41C>T
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13387
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

3-140675575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675575
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675575
    reference: chr 3
allele count: 14
allele frequency: 1.194967479813585e-4
allele num: 117158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.460G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+42G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+42G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

3-140675583-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675583
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675583
    reference: chr 3
allele count: 1
allele frequency: 8.594461728861921e-6
allele num: 116354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.468G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+50G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+50G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

3-140675583-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140675583
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140675583
    reference: chr 3
allele count: 7679
allele frequency: 6.599687161593069e-2
allele num: 116354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.206+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.408+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.206+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.206+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000502756
  gene symbol: SLC25A36
  hgvsc: ENST00000502756.1:n.468G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.56+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.206+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+50G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.56+50G>T
  variant of: http://identifiers.org/hgnc/25554
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 7.75e1
  variant carriers: 557
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 5.25e1
  variant carriers: 681
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 4.25e1
  variant carriers: 347
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 7.5e0
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 747
genotype depth: GenotypeDepth
  all individuals: 10002
  bin: 3.25e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 11786
  bin: 2.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 8.75e1
  variant carriers: 277
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 9.75e1
  variant carriers: 697
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.25e1
  variant carriers: 661
genotype depth: GenotypeDepth
  all individuals: 9944
  bin: 2.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 5.75e1
  variant carriers: 737
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.25e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 4.75e1
  variant carriers: 480
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 3.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 6.25e1
  variant carriers: 800
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 1.75e1
  variant carriers: 6
num of homozygotes: 320
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

3-140678255-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678255
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678255
    reference: chr 3
allele count: 1
allele frequency: 3.623188405797101e-5
allele num: 27600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-50T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-50T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-50T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2722T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-50T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-50T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2722T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-50T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2722T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-50T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21802
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-140678256-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678256
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678256
    reference: chr 3
allele count: 1
allele frequency: 3.602824614497767e-5
allele num: 27756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-49A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-49A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-49A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-49A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-49A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2723A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2723A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-49A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2723A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-49A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4640
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7306
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/3-140678261-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678261
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678261
    reference: chr 3
allele count: 2
allele frequency: 7.158196134574088e-5
allele num: 27940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2728A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2728A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-44A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2728A>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13821
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-140678270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678270
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678270
    reference: chr 3
allele count: 1
allele frequency: 3.491620111731843e-5
allele num: 28640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-35G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2737G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2737G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-35G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-35G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2737G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-35G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-35G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-35G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-35G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-140678275-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678275
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678275
    reference: chr 3
allele count: 1
allele frequency: 3.416000546560088e-5
allele num: 29274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-30T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-30T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-30T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2742T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-30T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2742T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2742T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-30T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-30T>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-30T>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-140678285-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678285
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678286
    reference: chr 3
allele count: 1
allele frequency: 3.24654243230959e-5
allele num: 30802
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-12dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-12dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-12dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-12dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2760dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-12dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2760dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-12dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2760dupT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-12dupT
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31197
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-140678298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678298
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678298
    reference: chr 3
allele count: 2
allele frequency: 5.457025920873124e-5
allele num: 36650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2765C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-7C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2765C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-7C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-7C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2765C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-7C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-7C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-7C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-7C>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
hgvs: c.207-7C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-140678301-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678301
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678301
    reference: chr 3
allele count: 13
allele frequency: 3.408495018353435e-4
allele num: 38140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.207-4T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.207-4T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2768T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.409-4T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.57-4T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.57-4T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.207-4T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2768T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2768T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.207-4T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33741
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 7.75e1
  variant carriers: 1
hgvs: c.207-4T>C
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

3-140678308-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678308
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678308
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 42912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.210G>T
  hgvsp: ENST00000502594.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.60G>T
  hgvsp: ENST00000512023.1:c.60G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.210G>T
  hgvsp: ENST00000446041.2:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.210G>T
  hgvsp: ENST00000507429.1:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2775G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.210G>T
  hgvsp: ENST00000324194.6:c.210G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2775G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2775G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.60G>T
  hgvsp: ENST00000512506.1:c.60G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.412G>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32948
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val70Val
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

3-140678326-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678326
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678326
    reference: chr 3
allele count: 1
allele frequency: 2.038237332354979e-5
allele num: 49062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.228G>T
  hgvsp: ENST00000446041.2:c.228G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.78G>T
  hgvsp: ENST00000512506.1:c.78G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.228G>T
  hgvsp: ENST00000502594.1:c.228G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.430G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2793G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2793G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.228G>T
  hgvsp: ENST00000507429.1:c.228G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2793G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.228G>T
  hgvsp: ENST00000324194.6:c.228G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.78G>T
  hgvsp: ENST00000512023.1:c.78G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly76Gly
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

3-140678341-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678341
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678341
    reference: chr 3
allele count: 1
allele frequency: 1.959017356893782e-5
allele num: 51046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2808T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.243T>C
  hgvsp: ENST00000324194.6:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.243T>C
  hgvsp: ENST00000446041.2:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2808T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.93T>C
  hgvsp: ENST00000512506.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.243T>C
  hgvsp: ENST00000507429.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.445T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.93T>C
  hgvsp: ENST00000512023.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2808T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.243T>C
  hgvsp: ENST00000502594.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe81Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

3-140678341-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678341
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678341
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 51046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2808T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.93T>G
  hgvsp: ENSP00000424505.1:p.Phe31Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2808T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2808T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.93T>G
  hgvsp: ENSP00000423711.1:p.Phe31Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.243T>G
  hgvsp: ENSP00000423319.1:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.243T>G
  hgvsp: ENSP00000320688.6:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.243T>G
  hgvsp: ENSP00000421470.1:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.445T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.243T>G
  hgvsp: ENSP00000401938.2:p.Phe81Leu
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 28260
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe81Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

3-140678355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678355
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678355
    reference: chr 3
allele count: 1
allele frequency: 1.936108422071636e-5
allele num: 51650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2822C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.459C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.257C>T
  hgvsp: ENSP00000421470.1:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2822C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.257C>T
  hgvsp: ENSP00000423319.1:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.257C>T
  hgvsp: ENSP00000401938.2:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.107C>T
  hgvsp: ENSP00000423711.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.107C>T
  hgvsp: ENSP00000424505.1:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.257C>T
  hgvsp: ENSP00000320688.6:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2822C>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9568
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro86Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

3-140678358-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678358
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678358
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 51886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.110A>G
  hgvsp: ENSP00000424505.1:p.Asn37Ser
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.110A>G
  hgvsp: ENSP00000423711.1:p.Asn37Ser
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2825A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.260A>G
  hgvsp: ENSP00000320688.6:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.260A>G
  hgvsp: ENSP00000423319.1:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2825A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.462A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.260A>G
  hgvsp: ENSP00000401938.2:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.260A>G
  hgvsp: ENSP00000421470.1:p.Asn87Ser
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2825A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25776
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn87Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

3-140678362-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678362
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678362
    reference: chr 3
allele count: 1
allele frequency: 1.967419532541119e-5
allele num: 50828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2829A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.466A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.264A>G
  hgvsp: ENST00000446041.2:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.264A>G
  hgvsp: ENST00000502594.1:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2829A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.264A>G
  hgvsp: ENST00000324194.6:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.264A>G
  hgvsp: ENST00000507429.1:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.114A>G
  hgvsp: ENST00000512506.1:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.114A>G
  hgvsp: ENST00000512023.1:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2829A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu88Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-140678364-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678364
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678364
    reference: chr 3
allele count: 2
allele frequency: 4.190412336573919e-5
allele num: 47728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2831T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.266T>G
  hgvsp: ENSP00000423319.1:p.Val89Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2831T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.468T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.116T>G
  hgvsp: ENSP00000424505.1:p.Val39Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.116T>G
  hgvsp: ENSP00000423711.1:p.Val39Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.266T>G
  hgvsp: ENSP00000421470.1:p.Val89Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.266T>G
  hgvsp: ENSP00000320688.6:p.Val89Gly
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2831T>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.266T>G
  hgvsp: ENSP00000401938.2:p.Val89Gly
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 24066
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11715
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val89Gly
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

3-140678369-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678369
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678369
    reference: chr 3
allele count: 1
allele frequency: 1.965872454195172e-5
allele num: 50868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2836G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.271G>A
  hgvsp: ENSP00000421470.1:p.Val91Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.121G>A
  hgvsp: ENSP00000424505.1:p.Val41Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.121G>A
  hgvsp: ENSP00000423711.1:p.Val41Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.271G>A
  hgvsp: ENSP00000320688.6:p.Val91Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.271G>A
  hgvsp: ENSP00000401938.2:p.Val91Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.271G>A
  hgvsp: ENSP00000423319.1:p.Val91Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.473G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2836G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2836G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23924
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val91Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

3-140678384-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678385
    reference: chr 3
allele count: 1097
allele frequency: 5.33041788143829e-2
allele num: 20580
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2866dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+17dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2866dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2866dupA
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22979
  bin: 7.5e0
  variant carriers: 547
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 365
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 2.5e0
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 1.75e1
  variant carriers: 303
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 110
hgvs: c.284+17dupA
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

3-140678384-T-TAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678386
    reference: chr 3
allele count: 19
allele frequency: 9.232264334305151e-4
allele num: 20580
alternate allele: TAA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+16_284+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+16_284+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+16_284+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+16_486+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+16_134+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2865_393+2866dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+16_134+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2865_206+2866dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+16_284+17dupAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2865_56+2866dupAA
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22979
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29798
  bin: 2.5e0
  variant carriers: 3
hgvs: c.284+16_284+17dupAA
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-140678384-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678383
    reference: chr 3
allele count: 8219
allele frequency: 3.993683187560739e-1
allele num: 20580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2866delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2866delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+17delA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2866delA
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22979
  bin: 7.5e0
  variant carriers: 3667
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 1.75e1
  variant carriers: 1257
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 470
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 1193
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 2.5e0
  variant carriers: 321
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 1570
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 363
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 2278
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 678
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 3.75e1
  variant carriers: 531
hgvs: c.284+17delA
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: TA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

3-140678384-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678382
    reference: chr 3
allele count: 334
allele frequency: 1.622934888241011e-2
allele num: 20580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+16_284+17delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+16_486+17delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+16_134+17delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+16_284+17delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2865_56+2866delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+16_284+17delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+16_284+17delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2865_393+2866delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2865_206+2866delAA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+16_134+17delAA
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22979
  bin: 7.5e0
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 1.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 24
hgvs: c.284+16_284+17delAA
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: TAA
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

3-140678384-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678381
    reference: chr 3
allele count: 16
allele frequency: 7.774538386783285e-4
allele num: 20580
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22979
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6169
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29798
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1214
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 3
  allele frequency: 3.218884120171674e-3
  allele num: 932
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1968
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 3
  allele frequency: 3.209929381553606e-4
  allele num: 9346
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
reference allele: TAAA
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

3-140678394-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678394
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678394
    reference: chr 3
allele count: 1
allele frequency: 2.959455460195324e-5
allele num: 33790
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2861A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2861A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+12A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2861A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22783
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  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: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-140678407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678407
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678407
    reference: chr 3
allele count: 1
allele frequency: 4.089310542242578e-5
allele num: 24454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2874A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2874A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+25A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2874A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2050
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-140678431-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140678431
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140678430
    reference: chr 3
allele count: 1
allele frequency: 5.243838489774515e-5
allele num: 19070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.134+52delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.284+52delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.134+52delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.284+52delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.393+2901delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.284+52delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.56+2901delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.486+52delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.206+2901delT
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.284+52delT
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6820
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: GT
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

3-140681922-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681922
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681923
    reference: chr 3
allele count: 2
allele frequency: 1.840705358293298e-5
allele num: 108654
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-46dupA
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-46dupA
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12332
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5825
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-140681924-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681924
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681924
    reference: chr 3
allele count: 1
allele frequency: 9.247614115558185e-6
allele num: 108136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-45C>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-45C>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16789
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4680
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

3-140681924-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681924
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681924
    reference: chr 3
allele count: 5
allele frequency: 4.623807057779093e-5
allele num: 108136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-45C>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-45C>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14149
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16789
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-140681925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681925
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681925
    reference: chr 3
allele count: 29
allele frequency: 2.669759905729857e-4
allele num: 108624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-44G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-44G>A
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13755
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18643
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8623
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5448
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

3-140681925-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681925
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681925
    reference: chr 3
allele count: 1
allele frequency: 9.206068640447784e-6
allele num: 108624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-44G>T
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-44G>T
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6046
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-140681936-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681936
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681936
    reference: chr 3
allele count: 1
allele frequency: 9.039302888961204e-6
allele num: 110628
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-33A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-33A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

3-140681943-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681943
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681943
    reference: chr 3
allele count: 3
allele frequency: 2.667804930103511e-5
allele num: 112452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-26T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-26T>C
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8540
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4302
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-140681949-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681949
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681950
    reference: chr 3
allele count: 2
allele frequency: 1.748618591312863e-5
allele num: 114376
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-20_135-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-20_135-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-20_57-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-20_285-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-20_394-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-20_487-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-20_207-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-20_285-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-20_285-19insC
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-20_285-19insC
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35421
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

3-140681962-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681962
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681962
    reference: chr 3
allele count: 3
allele frequency: 2.546862265688671e-5
allele num: 117792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.135-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.135-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.285-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.394-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.207-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.57-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.487-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.285-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.285-7A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.285-7A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.285-7A>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/3-140681972-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140681972
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140681972
    reference: chr 3
allele count: 1
allele frequency: 8.373245805003851e-6
allele num: 119428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.138A>C
  hgvsp: ENST00000512506.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.288A>C
  hgvsp: ENST00000507429.1:c.288A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.60A>C
  hgvsp: ENST00000513887.1:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.288A>C
  hgvsp: ENST00000502594.1:c.288A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.288A>C
  hgvsp: ENST00000446041.2:c.288A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.210A>C
  hgvsp: ENST00000453248.2:c.210A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.288A>C
  hgvsp: ENST00000324194.6:c.288A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.397A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.490A>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.138A>C
  hgvsp: ENST00000512023.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala96Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-140682007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140682007
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140682007
    reference: chr 3
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.323A>G
  hgvsp: ENSP00000320688.6:p.Lys108Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.323A>G
  hgvsp: ENSP00000401938.2:p.Lys108Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.323A>G
  hgvsp: ENSP00000421470.1:p.Lys108Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.323A>G
  hgvsp: ENSP00000423319.1:p.Lys108Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.432A>G
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.95A>G
  hgvsp: ENSP00000422265.1:p.Lys32Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.245A>G
  hgvsp: ENSP00000391521.2:p.Lys82Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.173A>G
  hgvsp: ENSP00000424505.1:p.Lys58Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.173A>G
  hgvsp: ENSP00000423711.1:p.Lys58Arg
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.525A>G
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys108Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-140682015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140682015
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140682015
    reference: chr 3
allele count: 6
allele frequency: 4.965078944755222e-5
allele num: 120844
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.331G>A
  hgvsp: ENSP00000320688.6:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.103G>A
  hgvsp: ENSP00000422265.1:p.Asp35Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.331G>A
  hgvsp: ENSP00000423319.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.253G>A
  hgvsp: ENSP00000391521.2:p.Asp85Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.181G>A
  hgvsp: ENSP00000424505.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.331G>A
  hgvsp: ENSP00000421470.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.440G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.533G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.181G>A
  hgvsp: ENSP00000423711.1:p.Asp61Asn
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.331G>A
  hgvsp: ENSP00000401938.2:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp111Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS

3-140682017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140682017
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140682017
    reference: chr 3
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.255T>C
  hgvsp: ENST00000453248.2:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.105T>C
  hgvsp: ENST00000513887.1:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.333T>C
  hgvsp: ENST00000324194.6:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.333T>C
  hgvsp: ENST00000446041.2:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.333T>C
  hgvsp: ENST00000502594.1:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.183T>C
  hgvsp: ENST00000512506.1:c.183T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.183T>C
  hgvsp: ENST00000512023.1:c.183T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.535T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.442T>C
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.333T>C
  hgvsp: ENST00000507429.1:c.333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39098
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp111Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

3-140682018-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140682018
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 140682018
    reference: chr 3
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000422265
  ensembl transcript: ENST00000513887
  gene symbol: SLC25A36
  hgvsc: ENST00000513887.1:c.106G>A
  hgvsp: ENSP00000422265.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423711
  ensembl transcript: ENST00000512506
  gene symbol: SLC25A36
  hgvsc: ENST00000512506.1:c.184G>A
  hgvsp: ENSP00000423711.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000393015
  gene symbol: SLC25A36
  hgvsc: ENST00000393015.4:n.536G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000320688
  ensembl transcript: ENST00000324194
  gene symbol: SLC25A36
  hgvsc: ENST00000324194.6:c.334G>A
  hgvsp: ENSP00000320688.6:p.Val112Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114120
  ensembl transcript: ENST00000515813
  gene symbol: SLC25A36
  hgvsc: ENST00000515813.1:n.443G>A
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000424505
  ensembl transcript: ENST00000512023
  gene symbol: SLC25A36
  hgvsc: ENST00000512023.1:c.184G>A
  hgvsp: ENSP00000424505.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000423319
  ensembl transcript: ENST00000502594
  gene symbol: SLC25A36
  hgvsc: ENST00000502594.1:c.334G>A
  hgvsp: ENSP00000423319.1:p.Val112Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000401938
  ensembl transcript: ENST00000446041
  gene symbol: SLC25A36
  hgvsc: ENST00000446041.2:c.334G>A
  hgvsp: ENSP00000401938.2:p.Val112Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000421470
  ensembl transcript: ENST00000507429
  gene symbol: SLC25A36
  hgvsc: ENST00000507429.1:c.334G>A
  hgvsp: ENSP00000421470.1:p.Val112Ile
  variant of: http://identifiers.org/hgnc/25554
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114120
  ensembl protein: ENSP00000391521
  ensembl transcript: ENST00000453248
  gene symbol: SLC25A36
  hgvsc: ENST00000453248.2:c.256G>A
  hgvsp: ENSP00000391521.2:p.Val86Ile
  variant of: http://identifiers.org/hgnc/25554
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val112Ile
num of homozygotes: 0
reference allele: G

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

GenotypeQuality
all individuals: 6712
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29082
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 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: 66672
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 2.003001e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 7.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.727e0

QD
type: SiteQuality
SIO_000300: 1.155e1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.807e0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10921
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 29074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6714
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2934
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 16498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

DP
type: SiteQuality
SIO_000300: 2.00325e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.658e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 1.219e0

QD
type: SiteQuality
SIO_000300: 8.51e0

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10926
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3672
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29082
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2320
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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: 908
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.421e0

DP
type: SiteQuality
SIO_000300: 2.003537e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

FS
type: SiteQuality
SIO_000300: 6.26e0

MQ
type: SiteQuality
SIO_000300: 5.791e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.78e1

GenotypeQuality
all individuals: 29059
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3296
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6759
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1662
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
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South Asian
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allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.188e0

MQRankSum
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SIO_000300: -7.97e-1

VQSLOD
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DP
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SIO_000300: 2.006968e6

MQ
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SIO_000300: 5.692e1

QD
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SIO_000300: 1.69e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.51e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

African
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allele count: 39
allele frequency: 3.748558246828143e-3
allele num: 10404
num of homozygotes: 0

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

Latino
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allele count: 4
allele frequency: 3.459609064175748e-4
allele num: 11562
num of homozygotes: 0

Other
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MQRankSum
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SIO_000300: -7.97e-1

VQSLOD
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MQ
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: 6.81e-1

ClippingRankSum
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DP
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SIO_000300: 2.006968e6

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

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

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

East Asian
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allele count: 0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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SIO_000300: -2.537e0

FS
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SIO_000300: 2.304e0

QD
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MQRankSum
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DP
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SIO_000300: 2.005436e6

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.893e1

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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variant carriers: 2

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

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

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

South Asian
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allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.005567e6

MQ
type: SiteQuality
SIO_000300: 5.92e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 3.24e0

BaseQRankSum
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SIO_000300: 4.32e0

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.347e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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 count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

South Asian
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allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.951e1

QD
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 6.49e-1

GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 5
allele frequency: 3.033244358165494e-4
allele num: 16484
num of homozygotes: 0

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 10
allele frequency: 1.498935755613514e-4
allele num: 66714
num of homozygotes: 0

East Asian
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allele count: 162
allele frequency: 1.872399445214979e-2
allele num: 8652
num of homozygotes: 4

Latino
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allele count: 82
allele frequency: 7.092198581560284e-3
allele num: 11562
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

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

European (Finnish)
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South Asian
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num of homozygotes: 0

Latino
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num of homozygotes: 0

QD
type: SiteQuality
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele count: 0
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allele num: 10406
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

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

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

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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
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East Asian
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VQSLOD
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QD
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MQRankSum
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MQ
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BaseQRankSum
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FS
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SIO_000300: 1.37e0

InbreedingCoeff
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SIO_000300: 1.11e-2

DP
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SIO_000300: 2.011937e6

ClippingRankSum
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SIO_000300: 1.23e0

ReadPosRankSum
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SIO_000300: 1.23e0

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

South Asian
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allele count: 1
allele frequency: 6.113964294448521e-5
allele num: 16356
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.14e0

MQ
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.349e1

DP
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SIO_000300: 2.011957e6

InbreedingCoeff
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SIO_000300: 8.800000000000001e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

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

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.00144023043687e-5
allele num: 66656
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South Asian
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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 2.85e-1

QD
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 5.905e1

VQSLOD
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SIO_000300: 1.34e0

ReadPosRankSum
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SIO_000300: 1.41e-1

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele count: 145
allele frequency: 1.675525768430784e-2
allele num: 8654
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.149305128520478e-5
allele num: 16262
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.2e-1

VQSLOD
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SIO_000300: 2.02e0

ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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SIO_000300: 1.199e1

BaseQRankSum
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SIO_000300: 1.13e-1

ReadPosRankSum
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SIO_000300: 5.02e-1

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.503422601176894e-5
allele num: 66616
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele count: 4
allele frequency: 2.460932693490833e-4
allele num: 16254
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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allele num: 8652
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European (Non-Finnish)
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DP
type: SiteQuality
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MQRankSum
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QD
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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SIO_000300: 3.41e-1

InbreedingCoeff
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SIO_000300: 8.1e-3

GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.103277060575968e-4
allele num: 16112
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

Other
type: Population
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African
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BaseQRankSum
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DP
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.898e1

GenotypeDepth
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.911558557410475e-4
allele num: 15694
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
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.884e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

ReadPosRankSum
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SIO_000300: 1.05e0

FS
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QD
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SIO_000300: 1.299e1

InbreedingCoeff
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SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.046e-1

DP
type: SiteQuality
SIO_000300: 1.999929e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.027917398413371e-5
allele num: 66052
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14734
num of homozygotes: 0

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

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

ReadPosRankSum
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SIO_000300: 2.35e0

ClippingRankSum
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SIO_000300: -1.092e0

BaseQRankSum
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SIO_000300: -3.927e0

MQRankSum
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FS
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SIO_000300: 2.106e0

QD
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SIO_000300: 1.11e1

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-2

DP
type: SiteQuality
SIO_000300: 1.968776e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14746
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66054
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 2
allele frequency: 1.732201628269531e-4
allele num: 11546
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.163e1

InbreedingCoeff
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SIO_000300: 1.8e-3

ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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SIO_000300: 5.923e1

QD
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SIO_000300: 1.253e1

VQSLOD
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SIO_000300: -1.72e0

MQRankSum
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SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

GenotypeQuality
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variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14510
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: 11544
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65968
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 1.365e0

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 6.77e-1

BaseQRankSum
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SIO_000300: 3.98e0

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 1.963499e6

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

GenotypeQuality
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bin: 7.75e1
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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GenotypeQuality
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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: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
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: 882
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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QD
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.963344e6

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51851064475962e-5
allele num: 65854
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

East Asian
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Latino
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allele num: 11524
num of homozygotes: 0

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

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

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

African
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num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.200460829493088e-5
allele num: 13888
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.132e0

VQSLOD
type: SiteQuality
SIO_000300: -1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

FS
type: SiteQuality
SIO_000300: 1.988e0

DP
type: SiteQuality
SIO_000300: 1.956754e6

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
all individuals: 841
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1648
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2900
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10353
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23733
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3198
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7049
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
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: 10336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523925632429137e-5
allele num: 65620
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.662e1

VQSLOD
type: SiteQuality
SIO_000300: -1.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

DP
type: SiteQuality
SIO_000300: 1.954855e6

GenotypeQuality
all individuals: 23616
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2290
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2896
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7061
bin: 9.75e1
variant carriers: 14

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.066682920882604e-4
allele num: 65624
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: 4
allele frequency: 3.474635163307853e-4
allele num: 11512
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.207830438622314e-4
allele num: 13588
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.954494e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.396e0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.373e1

GenotypeQuality
all individuals: 2555
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9002
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20036
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13374
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3136
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2774
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
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: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528444349341241e-5
allele num: 65426
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.584e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.037e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.51e0

DP
type: SiteQuality
SIO_000300: 2.181741e6

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 2555
bin: 8.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1555
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 372
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2034
bin: 9.25e1
variant carriers: 18

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 9002
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 315
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 436
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 20036
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 532
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13374
bin: 9.75e1
variant carriers: 7318

GenotypeQuality
all individuals: 376
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3136
bin: 7.75e1
variant carriers: 12

GenotypeQuality
all individuals: 818
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1429
bin: 8.75e1
variant carriers: 21

GenotypeQuality
all individuals: 2774
bin: 7.25e1
variant carriers: 11

South Asian
type: Population
allele count: 469
allele frequency: 3.591667943023434e-2
allele num: 13058
num of homozygotes: 8

African
type: Population
allele count: 1184
allele frequency: 1.151302994943602e-1
allele num: 10284
num of homozygotes: 64

Other
type: Population
allele count: 66
allele frequency: 7.692307692307693e-2
allele num: 858
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 2897
allele frequency: 4.427903280041574e-2
allele num: 65426
num of homozygotes: 64

East Asian
type: Population
allele count: 1490
allele frequency: 1.729742280009287e-1
allele num: 8614
num of homozygotes: 108

Latino
type: Population
allele count: 814
allele frequency: 7.077030081724918e-2
allele num: 11502
num of homozygotes: 31

European (Finnish)
type: Population
allele count: 759
allele frequency: 1.147912885662432e-1
allele num: 6612
num of homozygotes: 40

VQSLOD
type: SiteQuality
SIO_000300: 5.51e0

DP
type: SiteQuality
SIO_000300: 2.181741e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.037e0

QD
type: SiteQuality
SIO_000300: 1.584e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

GenotypeQuality
all individuals: 16120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9098
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7371
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1309
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9280
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4574
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.467406380027739e-4
allele num: 2884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12508
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.91844e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.619e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.295e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 1.173e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.97e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 1415
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8357
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2807
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16468
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10278
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1660
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.431703204047217e-4
allele num: 1186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2904
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

DP
type: SiteQuality
SIO_000300: 7.9357e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.84e-2

QD
type: SiteQuality
SIO_000300: 1.523e1

MQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.687e-1

GenotypeQuality
all individuals: 6606
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5714
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
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variant carriers: 0

GenotypeQuality
all individuals: 4792
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variant carriers: 0

GenotypeQuality
all individuals: 17265
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.431906614785992e-4
allele num: 8224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1688
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

FS
type: SiteQuality
SIO_000300: 7.923e0

QD
type: SiteQuality
SIO_000300: 1.648e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.65e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.402e0

DP
type: SiteQuality
SIO_000300: 8.03886e5

MQ
type: SiteQuality
SIO_000300: 5.878e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e0

GenotypeQuality
all individuals: 367
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
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GenotypeQuality
all individuals: 269
bin: 8.25e1
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GenotypeQuality
all individuals: 2107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1488
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
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GenotypeQuality
all individuals: 375
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variant carriers: 0

GenotypeQuality
all individuals: 3201
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variant carriers: 0

GenotypeQuality
all individuals: 20685
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variant carriers: 0

GenotypeQuality
all individuals: 16379
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variant carriers: 0

GenotypeQuality
all individuals: 4064
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variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5068
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 3.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele num: 8278
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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VQSLOD
type: SiteQuality
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DP
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QD
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MQRankSum
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MQ
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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.27e-1

InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 7.524454477050414e-5
allele num: 13290
num of homozygotes: 0

FS
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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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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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 7.126567844925884e-5
allele num: 14032
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Other
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VQSLOD
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ClippingRankSum
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DP
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FS
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QD
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 1.175917215428034e-4
allele num: 17008
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.194e1

ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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MQ
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.74e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

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

Latino
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allele frequency: 3.894080996884735e-4
allele num: 2568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 10
allele frequency: 5.636343140570398e-4
allele num: 17742
num of homozygotes: 0

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

European (Finnish)
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allele count: 2
allele frequency: 1.265822784810127e-3
allele num: 1580
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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East Asian
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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MQRankSum
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DP
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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East Asian
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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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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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MQ
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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Latino
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African
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South Asian
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European (Non-Finnish)
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allele num: 24862
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
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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: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.68e0

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

DP
type: SiteQuality
SIO_000300: 1.011646e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.052e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.970144513260283e-5
allele num: 25188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 9.86299e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.146e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.035e-1

QD
type: SiteQuality
SIO_000300: 7.0e0

GenotypeQuality
all individuals: 1443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

QD
type: SiteQuality
SIO_000300: 1.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 1.986e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 9.78132e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
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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
all individuals: 1966
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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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
all individuals: 1346
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 95
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GenotypeQuality
all individuals: 1531
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4848
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.019160211985324e-4
allele num: 9812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.29e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.554e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

DP
type: SiteQuality
SIO_000300: 9.63683e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.86e-1

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
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variant carriers: 0

GenotypeQuality
all individuals: 25460
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 2545
bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1915
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variant carriers: 1

GenotypeQuality
all individuals: 121
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variant carriers: 1

GenotypeQuality
all individuals: 5329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2001
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variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.051524710830704e-3
allele num: 1902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4032
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.76e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 2.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.117e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

DP
type: SiteQuality
SIO_000300: 9.67679e5

VQSLOD
type: SiteQuality
SIO_000300: -1.196e1

FS
type: SiteQuality
SIO_000300: 4.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.38e-2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 238
bin: 8.25e1
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GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.031282754172378e-5
allele num: 24806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4356
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.584e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.86e-2

DP
type: SiteQuality
SIO_000300: 9.48463e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

GenotypeQuality
all individuals: 743
bin: 4.25e1
variant carriers: 171

GenotypeQuality
all individuals: 1277
bin: 5.75e1
variant carriers: 98

GenotypeQuality
all individuals: 1097
bin: 2.25e1
variant carriers: 124

GenotypeQuality
all individuals: 29798
bin: 2.5e0
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GenotypeQuality
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variant carriers: 167

GenotypeQuality
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bin: 3.75e1
variant carriers: 128

GenotypeQuality
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variant carriers: 110

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 153

GenotypeQuality
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bin: 7.75e1
variant carriers: 21

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 114

GenotypeQuality
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bin: 6.25e1
variant carriers: 68

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 48

GenotypeQuality
all individuals: 3125
bin: 9.75e1
variant carriers: 198

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 29

African
type: Population
allele count: 141
allele frequency: 7.164634146341463e-2
allele num: 1968
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 5.294117647058823e-2
allele num: 170
num of homozygotes: 0

Latino
type: Population
allele count: 40
allele frequency: 4.291845493562232e-2
allele num: 932
num of homozygotes: 0

East Asian
type: Population
allele count: 58
allele frequency: 4.777594728171335e-2
allele num: 1214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 40
allele frequency: 7.11743772241993e-2
allele num: 562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 572
allele frequency: 6.120265354162208e-2
allele num: 9346
num of homozygotes: 0

South Asian
type: Population
allele count: 237
allele frequency: 3.710081402629931e-2
allele num: 6388
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.276e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 3.04e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

DP
type: SiteQuality
SIO_000300: 6.85642e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1407
bin: 5.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 426
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GenotypeQuality
all individuals: 724
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 350
bin: 9.25e1
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GenotypeQuality
all individuals: 853
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1214
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 1.524390243902439e-3
allele num: 1968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 8.559811684142949e-4
allele num: 9346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 932
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 7.827175954915466e-4
allele num: 6388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.558718861209964e-3
allele num: 562
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.882352941176471e-3
allele num: 170
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.85642e5

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.276e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.04e0

GenotypeQuality
all individuals: 743
bin: 4.25e1
variant carriers: 520

GenotypeQuality
all individuals: 671
bin: 7.25e1
variant carriers: 594

GenotypeQuality
all individuals: 639
bin: 6.75e1
variant carriers: 523

GenotypeQuality
all individuals: 1097
bin: 2.25e1
variant carriers: 282

GenotypeQuality
all individuals: 657
bin: 2.75e1
variant carriers: 400

GenotypeQuality
all individuals: 853
bin: 3.25e1
variant carriers: 661

GenotypeQuality
all individuals: 1123
bin: 1.75e1
variant carriers: 332

GenotypeQuality
all individuals: 1465
bin: 1.25e1
variant carriers: 505

GenotypeQuality
all individuals: 29798
bin: 2.5e0
variant carriers: 187

GenotypeQuality
all individuals: 350
bin: 9.25e1
variant carriers: 321

GenotypeQuality
all individuals: 426
bin: 8.25e1
variant carriers: 366

GenotypeQuality
all individuals: 6169
bin: 7.5e0
variant carriers: 342

GenotypeQuality
all individuals: 648
bin: 7.75e1
variant carriers: 595

GenotypeQuality
all individuals: 3125
bin: 9.75e1
variant carriers: 2843

GenotypeQuality
all individuals: 1277
bin: 5.75e1
variant carriers: 1149

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 281

GenotypeQuality
all individuals: 684
bin: 6.25e1
variant carriers: 557

GenotypeQuality
all individuals: 899
bin: 4.75e1
variant carriers: 696

GenotypeQuality
all individuals: 1407
bin: 5.25e1
variant carriers: 1195

Latino
type: Population
allele count: 370
allele frequency: 3.969957081545064e-1
allele num: 932
num of homozygotes: 0

African
type: Population
allele count: 711
allele frequency: 3.61280487804878e-1
allele num: 1968
num of homozygotes: 0

East Asian
type: Population
allele count: 491
allele frequency: 4.044481054365733e-1
allele num: 1214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 210
allele frequency: 3.736654804270463e-1
allele num: 562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3672
allele frequency: 3.928953563021613e-1
allele num: 9346
num of homozygotes: 0

Other
type: Population
allele count: 71
allele frequency: 4.176470588235294e-1
allele num: 170
num of homozygotes: 0

South Asian
type: Population
allele count: 2694
allele frequency: 4.217282404508453e-1
allele num: 6388
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.276e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

QD
type: SiteQuality
SIO_000300: 3.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.85642e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 38

GenotypeQuality
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bin: 7.5e0
variant carriers: 55

GenotypeQuality
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bin: 6.25e1
variant carriers: 26

GenotypeQuality
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variant carriers: 39

GenotypeQuality
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variant carriers: 28

GenotypeQuality
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bin: 3.25e1
variant carriers: 25

GenotypeQuality
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variant carriers: 26

GenotypeQuality
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variant carriers: 23

GenotypeQuality
all individuals: 1277
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variant carriers: 23

GenotypeQuality
all individuals: 724
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variant carriers: 20

GenotypeQuality
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variant carriers: 25

GenotypeQuality
all individuals: 350
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variant carriers: 12

GenotypeQuality
all individuals: 29798
bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
variant carriers: 16

GenotypeQuality
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variant carriers: 22

GenotypeQuality
all individuals: 426
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variant carriers: 31

GenotypeQuality
all individuals: 639
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variant carriers: 24

GenotypeQuality
all individuals: 3125
bin: 9.75e1
variant carriers: 74

GenotypeQuality
all individuals: 671
bin: 7.25e1
variant carriers: 26

European (Non-Finnish)
type: Population
allele count: 105
allele frequency: 1.123475283543762e-2
allele num: 9346
num of homozygotes: 0

South Asian
type: Population
allele count: 188
allele frequency: 2.943018159048215e-2
allele num: 6388
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 2.941176470588235e-2
allele num: 170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.338078291814947e-3
allele num: 562
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 5.589430894308943e-3
allele num: 1968
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 9.884678747940691e-3
allele num: 1214
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.072961373390558e-2
allele num: 932
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.276e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.85642e5

South Asian
type: Population
allele count: 10
allele frequency: 1.565435190983093e-3
allele num: 6388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

DP
type: SiteQuality
SIO_000300: 6.85642e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.276e-1

QD
type: SiteQuality
SIO_000300: 3.04e0

GenotypeQuality
all individuals: 1242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2344
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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
all individuals: 57
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.271951831409934e-5
allele num: 15944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.19199e5

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 3.757e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.271e0

VQSLOD
type: SiteQuality
SIO_000300: -1.983e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.08e-2

MQ
type: SiteQuality
SIO_000300: 5.706e1

QD
type: SiteQuality
SIO_000300: 1.567e1

GenotypeQuality
all individuals: 111
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 2509
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variant carriers: 0

GenotypeQuality
all individuals: 28787
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variant carriers: 0

GenotypeQuality
all individuals: 11436
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 1796
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variant carriers: 0

GenotypeQuality
all individuals: 1574
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 171
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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: 541
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GenotypeQuality
all individuals: 568
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.909479686386316e-5
allele num: 11224
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.044e0

QD
type: SiteQuality
SIO_000300: 1.572e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 4.94146e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.68e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.386e0

GenotypeQuality
all individuals: 4718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 1453
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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: 1109
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GenotypeQuality
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GenotypeQuality
all individuals: 373
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GenotypeQuality
all individuals: 5365
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GenotypeQuality
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GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 85
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.659475605708596e-4
allele num: 6026
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.79e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.785e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.395e0

ClippingRankSum
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SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 4.30096e5

MQ
type: SiteQuality
SIO_000300: 5.878e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 268
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GenotypeQuality
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variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.686568171085475e-5
allele num: 59292
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.078515962036238e-4
allele num: 9272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

FS
type: SiteQuality
SIO_000300: 2.229e0

DP
type: SiteQuality
SIO_000300: 1.204536e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.32e1

MQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

GenotypeQuality
all individuals: 4234
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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
all individuals: 1996
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 441
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GenotypeQuality
all individuals: 6321
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.693939085950469e-5
allele num: 59034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13962
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

DP
type: SiteQuality
SIO_000300: 1.219122e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 767
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GenotypeQuality
all individuals: 401
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.775756343801877e-5
allele num: 59034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.162297665090961e-5
allele num: 13962
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

DP
type: SiteQuality
SIO_000300: 1.219122e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 29

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

South Asian
type: Population
allele count: 4
allele frequency: 2.828854314002829e-4
allele num: 14140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.881725511375144e-4
allele num: 59252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.838911364472232e-4
allele num: 10876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.275e1

DP
type: SiteQuality
SIO_000300: 1.233907e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

VQSLOD
type: SiteQuality
SIO_000300: 5.22e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.194556822361162e-5
allele num: 10876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

DP
type: SiteQuality
SIO_000300: 1.233907e6

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.656342134031205e-5
allele num: 60374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10998
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.954e0

DP
type: SiteQuality
SIO_000300: 1.33625e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.992e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

MQ
type: SiteQuality
SIO_000300: 5.832e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.881382407497803e-5
allele num: 61458
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.91e-1

DP
type: SiteQuality
SIO_000300: 1.394529e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.969e0

MQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

QD
type: SiteQuality
SIO_000300: 1.696e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.194479938665985e-5
allele num: 62608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.255e0

MQRankSum
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SIO_000300: 4.62e-1

ReadPosRankSum
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QD
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.821453775582216e-5
allele num: 11336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.093293739173472e-5
allele num: 64656
num of homozygotes: 0

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

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

South Asian
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.495897e6

GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65586
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
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allele frequency: 0.0e0
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Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.898e1

ClippingRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -1.532e0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49306
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 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: 16476
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.145e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

FS
type: SiteQuality
SIO_000300: 1.346e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

DP
type: SiteQuality
SIO_000300: 1.542801e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e0

GenotypeQuality
all individuals: 1160
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49265
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6403
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010416039496658e-5
allele num: 66436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.735207357279195e-4
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.94325689856199e-4
allele num: 10292
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: 902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.038e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.048e0

DP
type: SiteQuality
SIO_000300: 1.543248e6

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 1.114e0

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

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1156
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1064
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49298
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.467e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: -4.336e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

DP
type: SiteQuality
SIO_000300: 1.543293e6