11-65146805-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146805
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146805
    reference: chr 11
allele count: 1
allele frequency: 8.419492809753141e-6
allele num: 118772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+533T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+42T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+533T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3120T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-65146811-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146811
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146811
    reference: chr 11
allele count: 1
allele frequency: 8.417933565668301e-6
allele num: 118794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+527T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3114T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+36T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+527T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

11-65146817-C-CAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146817
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146819
    reference: chr 11
allele count: 1
allele frequency: 8.413825598223e-6
allele num: 118852
alternate allele: CAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+520_153+521insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+29_267+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+29_213+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+29_339+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3107_3108insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+29_213+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+520_27+521insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+29_*393+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+29_267+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+29_339+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+29_339+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+29_*268+30insAT
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+29_*268+30insAT
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12220
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-65146818-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146818
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146818
    reference: chr 11
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3107G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+520G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+520G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+29G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+29G>T
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

11-65146834-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146834
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146834
    reference: chr 11
allele count: 1
allele frequency: 8.38841727342885e-6
allele num: 119212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+504T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3091T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+504T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+13T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+13T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-65146837-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146837
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146838
    reference: chr 11
allele count: 1
allele frequency: 8.385462961410099e-6
allele num: 119254
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+500dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+500dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3087dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+9dupG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+9dupG
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 12566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-65146838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146838
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146838
    reference: chr 11
allele count: 1
allele frequency: 8.384056877441857e-6
allele num: 119274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+500G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3087G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267+9G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+500G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

11-65146847-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146847
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146847
    reference: chr 11
allele count: 1
allele frequency: 8.37436773523599e-6
allele num: 119412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.213G>C
  hgvsp: ENSP00000294187.6:p.Gln71His
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+491G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+491G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.267G>C
  hgvsp: ENSP00000353879.3:p.Gln89His
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.213G>C
  hgvsp: ENSP00000407530.2:p.Gln71His
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.339G>C
  hgvsp: ENSP00000431642.1:p.Gln113His
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*268G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*268G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*393G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.339G>C
  hgvsp: ENSP00000435489.1:p.Gln113His
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3078G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.339G>C
  hgvsp: ENSP00000381782.1:p.Gln113His
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.267G>C
  hgvsp: ENSP00000431769.1:p.Gln89His
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln113His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

11-65146853-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146853
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146853
    reference: chr 11
allele count: 1
allele frequency: 8.36638053645232e-6
allele num: 119526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.261C>T
  hgvsp: ENST00000360662.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*262C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.261C>T
  hgvsp: ENST00000534028.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.207C>T
  hgvsp: ENST00000294187.6:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*387C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.333C>T
  hgvsp: ENST00000530936.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.333C>T
  hgvsp: ENST00000527174.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.207C>T
  hgvsp: ENST00000417511.2:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*262C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3072C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+485C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+485C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.333C>T
  hgvsp: ENST00000398802.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe111Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/11-65146855-ACCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146855
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146852
    reference: chr 11
allele count: 1
allele frequency: 8.375349670848758e-6
allele num: 119398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.256_258delGGG
  hgvsp: ENSP00000431769.1:p.Gly86del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.202_204delGGG
  hgvsp: ENSP00000294187.6:p.Gly68del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.256_258delGGG
  hgvsp: ENSP00000353879.3:p.Gly86del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.328_330delGGG
  hgvsp: ENSP00000431642.1:p.Gly110del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.328_330delGGG
  hgvsp: ENSP00000435489.1:p.Gly110del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.202_204delGGG
  hgvsp: ENSP00000407530.2:p.Gly68del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*257_*259delGGG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*382_*384delGGG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*257_*259delGGG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.328_330delGGG
  hgvsp: ENSP00000381782.1:p.Gly110del
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+480_27+482delGGG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3067_3069delGGG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+480_153+482delGGG
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12479
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly110del
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: ACCC
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/11-65146856-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146856
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146856
    reference: chr 11
allele count: 4
allele frequency: 3.345376689415228e-5
allele num: 119568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.330G>T
  hgvsp: ENST00000527174.1:c.330G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.258G>T
  hgvsp: ENST00000534028.1:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.330G>T
  hgvsp: ENST00000398802.1:c.330G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+482G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.204G>T
  hgvsp: ENST00000294187.6:c.204G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3069G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*259G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.204G>T
  hgvsp: ENST00000417511.2:c.204G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.330G>T
  hgvsp: ENST00000530936.1:c.330G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*259G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+482G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*384G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.258G>T
  hgvsp: ENST00000360662.3:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly110Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-65146858-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146858
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146858
    reference: chr 11
allele count: 1
allele frequency: 8.35812911637859e-6
allele num: 119644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.328G>A
  hgvsp: ENSP00000431642.1:p.Gly110Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+480G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.328G>A
  hgvsp: ENSP00000381782.1:p.Gly110Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*257G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*257G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3067G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.202G>A
  hgvsp: ENSP00000407530.2:p.Gly68Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+480G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.256G>A
  hgvsp: ENSP00000353879.3:p.Gly86Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.256G>A
  hgvsp: ENSP00000431769.1:p.Gly86Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.328G>A
  hgvsp: ENSP00000435489.1:p.Gly110Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.202G>A
  hgvsp: ENSP00000294187.6:p.Gly68Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*382G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly110Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-65146859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146859
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146859
    reference: chr 11
allele count: 3
allele frequency: 2.507522567703109e-5
allele num: 119640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+479G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*256G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.327G>A
  hgvsp: ENST00000530936.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.201G>A
  hgvsp: ENST00000417511.2:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.201G>A
  hgvsp: ENST00000294187.6:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.255G>A
  hgvsp: ENST00000360662.3:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.327G>A
  hgvsp: ENST00000527174.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.327G>A
  hgvsp: ENST00000398802.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*381G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*256G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.255G>A
  hgvsp: ENST00000534028.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3066G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+479G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly109Gly
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: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

11-65146861-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146861
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146861
    reference: chr 11
allele count: 4
allele frequency: 3.343587000133743e-5
allele num: 119632
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.325G>A
  hgvsp: ENSP00000381782.1:p.Gly109Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+477G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.199G>A
  hgvsp: ENSP00000407530.2:p.Gly67Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.199G>A
  hgvsp: ENSP00000294187.6:p.Gly67Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*254G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.325G>A
  hgvsp: ENSP00000431642.1:p.Gly109Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.253G>A
  hgvsp: ENSP00000353879.3:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+477G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.253G>A
  hgvsp: ENSP00000431769.1:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3064G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*254G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.325G>A
  hgvsp: ENSP00000435489.1:p.Gly109Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*379G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly109Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

11-65146862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146862
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146862
    reference: chr 11
allele count: 2
allele frequency: 1.671262638923707e-5
allele num: 119670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3063C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.252C>T
  hgvsp: ENST00000534028.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.324C>T
  hgvsp: ENST00000398802.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.252C>T
  hgvsp: ENST00000360662.3:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.198C>T
  hgvsp: ENST00000294187.6:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*378C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.324C>T
  hgvsp: ENST00000530936.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+476C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.324C>T
  hgvsp: ENST00000527174.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.198C>T
  hgvsp: ENST00000417511.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+476C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr108Thr
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

11-65146866-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146866
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146866
    reference: chr 11
allele count: 3
allele frequency: 2.505093690504025e-5
allele num: 119756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+472G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.194G>A
  hgvsp: ENSP00000294187.6:p.Cys65Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.194G>A
  hgvsp: ENSP00000407530.2:p.Cys65Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.320G>A
  hgvsp: ENSP00000431642.1:p.Cys107Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.320G>A
  hgvsp: ENSP00000435489.1:p.Cys107Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+472G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*249G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.248G>A
  hgvsp: ENSP00000431769.1:p.Cys83Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.320G>A
  hgvsp: ENSP00000381782.1:p.Cys107Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3059G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*249G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.248G>A
  hgvsp: ENSP00000353879.3:p.Cys83Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*374G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys107Tyr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-65146870-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146870
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146870
    reference: chr 11
allele count: 1
allele frequency: 8.351428094204109e-6
allele num: 119740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.190G>T
  hgvsp: ENSP00000294187.6:p.Gly64Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*245G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.190G>T
  hgvsp: ENSP00000407530.2:p.Gly64Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.316G>T
  hgvsp: ENSP00000431642.1:p.Gly106Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.316G>T
  hgvsp: ENSP00000435489.1:p.Gly106Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.244G>T
  hgvsp: ENSP00000353879.3:p.Gly82Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+468G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.316G>T
  hgvsp: ENSP00000381782.1:p.Gly106Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.244G>T
  hgvsp: ENSP00000431769.1:p.Gly82Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*370G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3055G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*245G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+468G>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12515
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly106Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

11-65146871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146871
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146871
    reference: chr 11
allele count: 9
allele frequency: 7.512144633824683e-5
allele num: 119806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3054G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.189G>A
  hgvsp: ENST00000417511.2:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.243G>A
  hgvsp: ENST00000360662.3:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.315G>A
  hgvsp: ENST00000398802.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.189G>A
  hgvsp: ENST00000294187.6:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*244G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.243G>A
  hgvsp: ENST00000534028.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*369G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.315G>A
  hgvsp: ENST00000527174.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.315G>A
  hgvsp: ENST00000530936.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+467G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*244G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+467G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30087
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala105Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-65146879-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146879
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146879
    reference: chr 11
allele count: 89
allele frequency: 7.420005669217815e-4
allele num: 119946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.181T>C
  hgvsp: ENSP00000294187.6:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3046T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*361T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.181T>C
  hgvsp: ENSP00000407530.2:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.307T>C
  hgvsp: ENSP00000381782.1:p.Phe103Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+459T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*236T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.235T>C
  hgvsp: ENSP00000353879.3:p.Phe79Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.307T>C
  hgvsp: ENSP00000435489.1:p.Phe103Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+459T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.235T>C
  hgvsp: ENSP00000431769.1:p.Phe79Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.307T>C
  hgvsp: ENSP00000431642.1:p.Phe103Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*236T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12514
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Phe103Leu
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

11-65146883-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146883
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146883
    reference: chr 11
allele count: 1
allele frequency: 8.334861391255063e-6
allele num: 119978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+455C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.177C>T
  hgvsp: ENST00000417511.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.303C>T
  hgvsp: ENST00000527174.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.177C>T
  hgvsp: ENST00000294187.6:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.303C>T
  hgvsp: ENST00000530936.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*357C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.231C>T
  hgvsp: ENST00000534028.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*232C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*232C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.303C>T
  hgvsp: ENST00000398802.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3042C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.231C>T
  hgvsp: ENST00000360662.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+455C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His101His
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

11-65146887-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146887
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146887
    reference: chr 11
allele count: 1174
allele frequency: 9.784964160693448e-3
allele num: 119980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.173T>C
  hgvsp: ENSP00000407530.2:p.Met58Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.299T>C
  hgvsp: ENSP00000381782.1:p.Met100Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.299T>C
  hgvsp: ENSP00000435489.1:p.Met100Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*228T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*228T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.173T>C
  hgvsp: ENSP00000294187.6:p.Met58Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*353T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+451T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.299T>C
  hgvsp: ENSP00000431642.1:p.Met100Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.227T>C
  hgvsp: ENSP00000353879.3:p.Met76Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.227T>C
  hgvsp: ENSP00000431769.1:p.Met76Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+451T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3038T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29990
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Met100Thr
num of homozygotes: 63
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

11-65146896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146896
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146896
    reference: chr 11
allele count: 1
allele frequency: 8.330278897737497e-6
allele num: 120044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+442C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.290C>T
  hgvsp: ENSP00000381782.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.164C>T
  hgvsp: ENSP00000407530.2:p.Pro55Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3029C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*344C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.164C>T
  hgvsp: ENSP00000294187.6:p.Pro55Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.290C>T
  hgvsp: ENSP00000435489.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+442C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.290C>T
  hgvsp: ENSP00000431642.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.218C>T
  hgvsp: ENSP00000353879.3:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*219C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.218C>T
  hgvsp: ENSP00000431769.1:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro97Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-65146898-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146898
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146898
    reference: chr 11
allele count: 3
allele frequency: 2.50191813723855e-5
allele num: 119908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+440G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*217G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3027G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.216G>T
  hgvsp: ENST00000360662.3:c.216G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+440G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.288G>T
  hgvsp: ENST00000527174.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.162G>T
  hgvsp: ENST00000417511.2:c.162G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*217G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.288G>T
  hgvsp: ENST00000530936.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*342G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.162G>T
  hgvsp: ENST00000294187.6:c.162G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.216G>T
  hgvsp: ENST00000534028.1:c.216G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.288G>T
  hgvsp: ENST00000398802.1:c.288G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro96Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-65146898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146898
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146898
    reference: chr 11
allele count: 4
allele frequency: 3.3358908496514e-5
allele num: 119908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.288G>A
  hgvsp: ENST00000527174.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.162G>A
  hgvsp: ENST00000417511.2:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.216G>A
  hgvsp: ENST00000534028.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3027G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+440G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+440G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*217G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.162G>A
  hgvsp: ENST00000294187.6:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.288G>A
  hgvsp: ENST00000398802.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*342G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.216G>A
  hgvsp: ENST00000360662.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.288G>A
  hgvsp: ENST00000530936.1:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*217G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro96Pro
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

11-65146899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146899
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146899
    reference: chr 11
allele count: 3
allele frequency: 2.499791684026331e-5
allele num: 120010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.215C>T
  hgvsp: ENSP00000431769.1:p.Pro72Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.161C>T
  hgvsp: ENSP00000294187.6:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*216C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.161C>T
  hgvsp: ENSP00000407530.2:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3026C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*216C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.287C>T
  hgvsp: ENSP00000431642.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.215C>T
  hgvsp: ENSP00000353879.3:p.Pro72Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.287C>T
  hgvsp: ENSP00000381782.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+439C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.287C>T
  hgvsp: ENSP00000435489.1:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*341C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+439C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro96Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

11-65146902-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146902
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146902
    reference: chr 11
allele count: 1
allele frequency: 8.371283150281276e-6
allele num: 119456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+436A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.284A>G
  hgvsp: ENSP00000381782.1:p.Gln95Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.212A>G
  hgvsp: ENSP00000431769.1:p.Gln71Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.212A>G
  hgvsp: ENSP00000353879.3:p.Gln71Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.158A>G
  hgvsp: ENSP00000407530.2:p.Gln53Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.158A>G
  hgvsp: ENSP00000294187.6:p.Gln53Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*213A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.284A>G
  hgvsp: ENSP00000431642.1:p.Gln95Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3023A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+436A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.284A>G
  hgvsp: ENSP00000435489.1:p.Gln95Arg
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*213A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*338A>G
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30408
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln95Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-65146908-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146908
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146908
    reference: chr 11
allele count: 1
allele frequency: 8.316146630297385e-6
allele num: 120248
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.278G>C
  hgvsp: ENSP00000381782.1:p.Arg93Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.278G>C
  hgvsp: ENSP00000431642.1:p.Arg93Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.206G>C
  hgvsp: ENSP00000353879.3:p.Arg69Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.206G>C
  hgvsp: ENSP00000431769.1:p.Arg69Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+430G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*207G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3017G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.152G>C
  hgvsp: ENSP00000407530.2:p.Arg51Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.278G>C
  hgvsp: ENSP00000435489.1:p.Arg93Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+430G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.152G>C
  hgvsp: ENSP00000294187.6:p.Arg51Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*207G>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*332G>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31344
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg93Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-65146908-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146908
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146908
    reference: chr 11
allele count: 5
allele frequency: 4.158073315148693e-5
allele num: 120248
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.278G>A
  hgvsp: ENSP00000381782.1:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.206G>A
  hgvsp: ENSP00000431769.1:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+430G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.152G>A
  hgvsp: ENSP00000294187.6:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.278G>A
  hgvsp: ENSP00000435489.1:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*332G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.278G>A
  hgvsp: ENSP00000431642.1:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+430G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.152G>A
  hgvsp: ENSP00000407530.2:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.206G>A
  hgvsp: ENSP00000353879.3:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3017G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*207G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*207G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg93Gln
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

11-65146909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146909
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146909
    reference: chr 11
allele count: 3
allele frequency: 2.494429108324741e-5
allele num: 120268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*331C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.205C>T
  hgvsp: ENSP00000353879.3:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3016C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.151C>T
  hgvsp: ENSP00000407530.2:p.Arg51Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.277C>T
  hgvsp: ENSP00000431642.1:p.Arg93Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.151C>T
  hgvsp: ENSP00000294187.6:p.Arg51Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.205C>T
  hgvsp: ENSP00000431769.1:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+429C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.277C>T
  hgvsp: ENSP00000381782.1:p.Arg93Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.277C>T
  hgvsp: ENSP00000435489.1:p.Arg93Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*206C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*206C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+429C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg93Trp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS

11-65146910-CCG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146910
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146908
    reference: chr 11
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*203_*204delCG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*328_*329delCG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+426_27+427delCG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+426_153+427delCG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.148_149delCG
  hgvsp: ENSP00000407530.2:p.Arg50AlafsTer29
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.274_275delCG
  hgvsp: ENSP00000381782.1:p.Arg92AlafsTer29
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.274_275delCG
  hgvsp: ENSP00000435489.1:p.Arg92AlafsTer29
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*203_*204delCG
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.148_149delCG
  hgvsp: ENSP00000294187.6:p.Arg50AlafsTer29
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.202_203delCG
  hgvsp: ENSP00000353879.3:p.Arg68AlafsTer29
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.274_275delCG
  hgvsp: ENSP00000431642.1:p.Arg92AlafsTer?
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.202_203delCG
  hgvsp: ENSP00000431769.1:p.Arg68AlafsTer29
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3013_3014delCG
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg92AlafsTer29
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: CCG
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-65146911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146911
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146911
    reference: chr 11
allele count: 5
allele frequency: 4.1556541830815e-5
allele num: 120318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.149G>A
  hgvsp: ENSP00000294187.6:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*329G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.275G>A
  hgvsp: ENSP00000435489.1:p.Arg92Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.203G>A
  hgvsp: ENSP00000353879.3:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.203G>A
  hgvsp: ENSP00000431769.1:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3014G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+427G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+427G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*204G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.275G>A
  hgvsp: ENSP00000431642.1:p.Arg92Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.275G>A
  hgvsp: ENSP00000381782.1:p.Arg92Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.149G>A
  hgvsp: ENSP00000407530.2:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*204G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg92Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

11-65146912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146912
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146912
    reference: chr 11
allele count: 1
allele frequency: 8.311584686736373e-6
allele num: 120314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.274C>T
  hgvsp: ENSP00000435489.1:p.Arg92Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.202C>T
  hgvsp: ENSP00000353879.3:p.Arg68Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*328C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+426C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.148C>T
  hgvsp: ENSP00000294187.6:p.Arg50Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.202C>T
  hgvsp: ENSP00000431769.1:p.Arg68Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*203C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*203C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.148C>T
  hgvsp: ENSP00000407530.2:p.Arg50Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.274C>T
  hgvsp: ENSP00000381782.1:p.Arg92Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.274C>T
  hgvsp: ENSP00000431642.1:p.Arg92Trp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3013C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+426C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg92Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-65146913-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146913
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146913
    reference: chr 11
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.273G>T
  hgvsp: ENSP00000381782.1:p.Glu91Asp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.147G>T
  hgvsp: ENSP00000294187.6:p.Glu49Asp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*202G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.201G>T
  hgvsp: ENSP00000353879.3:p.Glu67Asp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.147G>T
  hgvsp: ENSP00000407530.2:p.Glu49Asp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+425G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.273G>T
  hgvsp: ENSP00000431642.1:p.Glu91Asp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.273G>T
  hgvsp: ENSP00000435489.1:p.Glu91Asp
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*202G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*327G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+425G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3012G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.201G>T
  hgvsp: ENSP00000431769.1:p.Glu67Asp
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu91Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

11-65146914-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146914
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146914
    reference: chr 11
allele count: 1
allele frequency: 8.308408109006315e-6
allele num: 120360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.146A>G
  hgvsp: ENSP00000294187.6:p.Glu49Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*326A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.272A>G
  hgvsp: ENSP00000435489.1:p.Glu91Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.200A>G
  hgvsp: ENSP00000353879.3:p.Glu67Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*201A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.272A>G
  hgvsp: ENSP00000431642.1:p.Glu91Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+424A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.200A>G
  hgvsp: ENSP00000431769.1:p.Glu67Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.272A>G
  hgvsp: ENSP00000381782.1:p.Glu91Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3011A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*201A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.146A>G
  hgvsp: ENSP00000407530.2:p.Glu49Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+424A>G
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu91Gly
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

11-65146915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146915
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146915
    reference: chr 11
allele count: 20
allele frequency: 1.661709234118214e-4
allele num: 120358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.271G>A
  hgvsp: ENSP00000435489.1:p.Glu91Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.271G>A
  hgvsp: ENSP00000431642.1:p.Glu91Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*200G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.145G>A
  hgvsp: ENSP00000294187.6:p.Glu49Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*325G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+423G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.199G>A
  hgvsp: ENSP00000431769.1:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.145G>A
  hgvsp: ENSP00000407530.2:p.Glu49Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.199G>A
  hgvsp: ENSP00000353879.3:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+423G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.271G>A
  hgvsp: ENSP00000381782.1:p.Glu91Lys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3010G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*200G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu91Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

11-65146916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146916
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146916
    reference: chr 11
allele count: 1
allele frequency: 8.307717869901138e-6
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.270G>A
  hgvsp: ENST00000398802.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*324G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3009G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+422G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.144G>A
  hgvsp: ENST00000294187.6:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.270G>A
  hgvsp: ENST00000530936.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.198G>A
  hgvsp: ENST00000534028.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.198G>A
  hgvsp: ENST00000360662.3:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.270G>A
  hgvsp: ENST00000527174.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.144G>A
  hgvsp: ENST00000417511.2:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+422G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln90Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-65146921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146921
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146921
    reference: chr 11
allele count: 7
allele frequency: 5.813374082317377e-5
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.139C>T
  hgvsp: ENSP00000407530.2:p.His47Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*194C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3004C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+417C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.139C>T
  hgvsp: ENSP00000294187.6:p.His47Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.265C>T
  hgvsp: ENSP00000381782.1:p.His89Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.265C>T
  hgvsp: ENSP00000435489.1:p.His89Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.193C>T
  hgvsp: ENSP00000353879.3:p.His65Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.265C>T
  hgvsp: ENSP00000431642.1:p.His89Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.193C>T
  hgvsp: ENSP00000431769.1:p.His65Tyr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+417C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*194C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*319C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12382
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His89Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-65146925-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146925
    reference: chr 11
allele count: 1
allele frequency: 8.303992559622666e-6
allele num: 120424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.189C>A
  hgvsp: ENST00000534028.1:c.189C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.261C>A
  hgvsp: ENST00000527174.1:c.261C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.135C>A
  hgvsp: ENST00000417511.2:c.135C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.3000C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*237C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.135C>A
  hgvsp: ENST00000294187.6:c.135C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.261C>A
  hgvsp: ENST00000530936.1:c.261C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.189C>A
  hgvsp: ENST00000360662.3:c.189C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*315C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.261C>A
  hgvsp: ENST00000398802.1:c.261C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+413C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+413C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*190C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*190C>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr87Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-65146928-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146928
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146928
    reference: chr 11
allele count: 1
allele frequency: 8.30357884248111e-6
allele num: 120430
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*187C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+410C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.186C>A
  hgvsp: ENST00000360662.3:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.258C>A
  hgvsp: ENST00000527174.1:c.258C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*253C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*187C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*312C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.258C>A
  hgvsp: ENST00000530936.1:c.258C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2997C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+410C>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.258C>A
  hgvsp: ENST00000398802.1:c.258C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.132C>A
  hgvsp: ENST00000417511.2:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.186C>A
  hgvsp: ENST00000534028.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.132C>A
  hgvsp: ENST00000294187.6:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*234C>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala86Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

11-65146931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146931
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146931
    reference: chr 11
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.129G>A
  hgvsp: ENST00000417511.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.255G>A
  hgvsp: ENST00000398802.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.255G>A
  hgvsp: ENST00000530936.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.129G>A
  hgvsp: ENST00000294187.6:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*309G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.183G>A
  hgvsp: ENST00000534028.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+407G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.674G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.183G>A
  hgvsp: ENST00000360662.3:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*184G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+407G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*231G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.255G>A
  hgvsp: ENST00000527174.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2994G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*184G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*250G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr85Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-65146935-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146935
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146935
    reference: chr 11
allele count: 2
allele frequency: 1.660164356271271e-5
allele num: 120470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.251T>C
  hgvsp: ENSP00000431642.1:p.Leu84Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.125T>C
  hgvsp: ENSP00000407530.2:p.Leu42Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.251T>C
  hgvsp: ENSP00000435489.1:p.Leu84Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.179T>C
  hgvsp: ENSP00000353879.3:p.Leu60Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*180T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2990T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.251T>C
  hgvsp: ENSP00000381782.1:p.Leu84Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*305T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*180T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.179T>C
  hgvsp: ENSP00000431769.1:p.Leu60Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.670T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*227T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+403T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.125T>C
  hgvsp: ENSP00000294187.6:p.Leu42Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+403T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*246T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu84Pro
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

11-65146944-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146944
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146943
    reference: chr 11
allele count: 2
allele frequency: 1.659999004000598e-5
allele num: 120482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.115delC
  hgvsp: ENSP00000294187.6:p.Leu39CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.169delC
  hgvsp: ENSP00000431769.1:p.Leu57CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.660delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*236delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+393delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.115delC
  hgvsp: ENSP00000407530.2:p.Leu39CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*295delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.241delC
  hgvsp: ENSP00000431642.1:p.Leu81CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.241delC
  hgvsp: ENSP00000435489.1:p.Leu81CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*170delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.241delC
  hgvsp: ENSP00000381782.1:p.Leu81CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*217delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.169delC
  hgvsp: ENSP00000353879.3:p.Leu57CysfsTer24
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+393delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*170delC
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2980delC
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu81CysfsTer24
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: AG
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/11-65146960-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146960
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146960
    reference: chr 11
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.100G>T
  hgvsp: ENSP00000294187.6:p.Val34Phe
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*280G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+378G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.100G>T
  hgvsp: ENSP00000407530.2:p.Val34Phe
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2965G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*202G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.226G>T
  hgvsp: ENSP00000435489.1:p.Val76Phe
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+378G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.154G>T
  hgvsp: ENSP00000431769.1:p.Val52Phe
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*221G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.226G>T
  hgvsp: ENSP00000431642.1:p.Val76Phe
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*155G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.226G>T
  hgvsp: ENSP00000381782.1:p.Val76Phe
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.645G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*155G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.154G>T
  hgvsp: ENSP00000353879.3:p.Val52Phe
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val76Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

11-65146965-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146965
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146965
    reference: chr 11
allele count: 49
allele frequency: 4.067537728487706e-4
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*150T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.221T>C
  hgvsp: ENSP00000381782.1:p.Phe74Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.149T>C
  hgvsp: ENSP00000353879.3:p.Phe50Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.95T>C
  hgvsp: ENSP00000407530.2:p.Phe32Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+373T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2960T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.221T>C
  hgvsp: ENSP00000431642.1:p.Phe74Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+373T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.221T>C
  hgvsp: ENSP00000435489.1:p.Phe74Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*275T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*216T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.149T>C
  hgvsp: ENSP00000431769.1:p.Phe50Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.95T>C
  hgvsp: ENSP00000294187.6:p.Phe32Ser
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.640T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*150T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*197T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe74Ser
num of homozygotes: 2
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

11-65146968-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146968
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146968
    reference: chr 11
allele count: 1
allele frequency: 8.301924386072691e-6
allele num: 120454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.92T>C
  hgvsp: ENSP00000294187.6:p.Leu31Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*213T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*147T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.218T>C
  hgvsp: ENSP00000435489.1:p.Leu73Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.218T>C
  hgvsp: ENSP00000381782.1:p.Leu73Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.146T>C
  hgvsp: ENSP00000353879.3:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.92T>C
  hgvsp: ENSP00000407530.2:p.Leu31Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.218T>C
  hgvsp: ENSP00000431642.1:p.Leu73Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+370T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*272T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.637T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+370T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*147T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.146T>C
  hgvsp: ENSP00000431769.1:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2957T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*194T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu73Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-65146974-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146974
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146974
    reference: chr 11
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.631C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2951C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*141C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.212C>G
  hgvsp: ENSP00000381782.1:p.Ser71Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.86C>G
  hgvsp: ENSP00000294187.6:p.Ser29Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.212C>G
  hgvsp: ENSP00000431642.1:p.Ser71Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*141C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.212C>G
  hgvsp: ENSP00000435489.1:p.Ser71Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.140C>G
  hgvsp: ENSP00000353879.3:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*266C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+364C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.140C>G
  hgvsp: ENSP00000431769.1:p.Ser47Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.86C>G
  hgvsp: ENSP00000407530.2:p.Ser29Cys
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*207C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*188C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+364C>G
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser71Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-65146989-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146989
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146989
    reference: chr 11
allele count: 10
allele frequency: 8.328891257995735e-5
allele num: 120064
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.197T>C
  hgvsp: ENSP00000435489.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*251T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.197T>C
  hgvsp: ENSP00000431642.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.71T>C
  hgvsp: ENSP00000294187.6:p.Ile24Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.125T>C
  hgvsp: ENSP00000353879.3:p.Ile42Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2936T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*192T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.197T>C
  hgvsp: ENSP00000381782.1:p.Ile66Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.616T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.71T>C
  hgvsp: ENSP00000407530.2:p.Ile24Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*126T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+349T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*173T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*126T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+349T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.125T>C
  hgvsp: ENSP00000431769.1:p.Ile42Thr
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile66Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum

11-65146998-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65146998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65146998
    reference: chr 11
allele count: 1
allele frequency: 8.354916868577158e-6
allele num: 119690
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.188T>C
  hgvsp: ENSP00000381782.1:p.Ile63Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2927T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.116T>C
  hgvsp: ENSP00000353879.3:p.Ile39Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.188T>C
  hgvsp: ENSP00000435489.1:p.Ile63Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.188T>C
  hgvsp: ENSP00000431642.1:p.Ile63Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.62T>C
  hgvsp: ENSP00000294187.6:p.Ile21Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*183T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.116T>C
  hgvsp: ENSP00000431769.1:p.Ile39Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*164T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+340T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*242T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*117T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.62T>C
  hgvsp: ENSP00000407530.2:p.Ile21Thr
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*117T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+340T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.607T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile63Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

11-65147000-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147000
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147000
    reference: chr 11
allele count: 1
allele frequency: 8.365820603342981e-6
allele num: 119534
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+338C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.605C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.60C>G
  hgvsp: ENST00000417511.2:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.186C>G
  hgvsp: ENST00000530936.1:c.186C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.114C>G
  hgvsp: ENST00000534028.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.186C>G
  hgvsp: ENST00000527174.1:c.186C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*162C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+338C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.186C>G
  hgvsp: ENST00000398802.1:c.186C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*240C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.60C>G
  hgvsp: ENST00000294187.6:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*181C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.114C>G
  hgvsp: ENST00000360662.3:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*115C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2925C>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*115C>G
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro62Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

11-65147005-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147005
    reference: chr 11
allele count: 9
allele frequency: 7.550969041026932e-5
allele num: 119190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.600T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.109T>C
  hgvsp: ENSP00000353879.3:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*176T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*110T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.55T>C
  hgvsp: ENSP00000407530.2:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+333T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.181T>C
  hgvsp: ENSP00000431642.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.181T>C
  hgvsp: ENSP00000435489.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.109T>C
  hgvsp: ENSP00000431769.1:p.Phe37Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.181T>C
  hgvsp: ENSP00000381782.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*235T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.55T>C
  hgvsp: ENSP00000294187.6:p.Phe19Leu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+333T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*110T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2920T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*157T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Phe61Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-65147006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147006
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147006
    reference: chr 11
allele count: 1
allele frequency: 8.395318770253707e-6
allele num: 119114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.180C>T
  hgvsp: ENST00000530936.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.54C>T
  hgvsp: ENST00000417511.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.180C>T
  hgvsp: ENST00000398802.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*175C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*109C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*234C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.108C>T
  hgvsp: ENST00000360662.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.180C>T
  hgvsp: ENST00000527174.1:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+332C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.54C>T
  hgvsp: ENST00000294187.6:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+332C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.108C>T
  hgvsp: ENST00000534028.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2919C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*109C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.599C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*156C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser60Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-65147008-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147008
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147008
    reference: chr 11
allele count: 1
allele frequency: 8.411419342899921e-6
allele num: 118886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.178A>G
  hgvsp: ENSP00000431642.1:p.Ser60Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.52A>G
  hgvsp: ENSP00000407530.2:p.Ser18Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.597A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*232A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+330A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.106A>G
  hgvsp: ENSP00000353879.3:p.Ser36Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2917A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.178A>G
  hgvsp: ENSP00000435489.1:p.Ser60Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*173A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.178A>G
  hgvsp: ENSP00000381782.1:p.Ser60Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.52A>G
  hgvsp: ENSP00000294187.6:p.Ser18Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.106A>G
  hgvsp: ENSP00000431769.1:p.Ser36Gly
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+330A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*107A>G
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser60Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

11-65147013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147013
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147013
    reference: chr 11
allele count: 387
allele frequency: 3.270514662384856e-3
allele num: 118330
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.173G>A
  hgvsp: ENSP00000381782.1:p.Gly58Glu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.101G>A
  hgvsp: ENSP00000431769.1:p.Gly34Glu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+325G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+325G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.47G>A
  hgvsp: ENSP00000407530.2:p.Gly16Glu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.101G>A
  hgvsp: ENSP00000353879.3:p.Gly34Glu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2912G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*227G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.173G>A
  hgvsp: ENSP00000435489.1:p.Gly58Glu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.173G>A
  hgvsp: ENSP00000431642.1:p.Gly58Glu
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*168G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.592G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.47G>A
  hgvsp: ENSP00000294187.6:p.Gly16Glu
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 12088
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 3.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
hgvs: p.Gly58Glu
num of homozygotes: 2
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

11-65147035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147035
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147035
    reference: chr 11
allele count: 1
allele frequency: 8.712319219376199e-6
allele num: 114780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2890C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+303C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-3C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+303C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10770
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.154-3C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

11-65147055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147055
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147055
    reference: chr 11
allele count: 3
allele frequency: 2.814839835613354e-5
allele num: 106578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+283G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2870G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+283G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-23G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-23G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

11-65147056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147056
    reference: chr 11
allele count: 38
allele frequency: 3.574922856927824e-4
allele num: 106296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2869C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+282C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+282C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-24C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-24C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15812
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-65147067-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147067
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147067
    reference: chr 11
allele count: 3
allele frequency: 3.019992349352715e-5
allele num: 99338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2858G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+271G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-35G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+271G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-35G>T
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8425
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-65147068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147068
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147068
    reference: chr 11
allele count: 2
allele frequency: 2.018937635016454e-5
allele num: 99062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2857C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+270C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-36C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+270C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-36C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

11-65147069-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147069
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147069
    reference: chr 11
allele count: 3
allele frequency: 3.031282838897421e-5
allele num: 98968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+269A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2856A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+269A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-37A>G
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-37A>G
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12283
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

11-65147079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147079
    reference: chr 11
allele count: 2
allele frequency: 2.178459393516905e-5
allele num: 91808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+259G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*83-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+259G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*130-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.154-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*208-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*149-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.573-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.28-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2846G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.154-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*83-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.28-47G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.154-47G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14667
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

11-65147292-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147292
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147292
    reference: chr 11
allele count: 1
allele frequency: 8.380965151946898e-6
allele num: 119318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*129+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.572+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*82+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*148+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2633T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.153+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-260T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-260T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*207+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.27+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*82+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.153+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.153+46T>C
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.27+46T>C
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

11-65147294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147294
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147294
    reference: chr 11
allele count: 54317
allele frequency: 4.573369931294625e-1
allele num: 118768
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.153+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-262C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2631C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.27+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*148+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*207+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*129+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.153+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.27+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-262C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*82+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.572+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.153+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*82+44C>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+44C>T
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 835
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 519
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.25e1
  variant carriers: 1334
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 344
genotype depth: GenotypeDepth
  all individuals: 11070
  bin: 3.25e1
  variant carriers: 7552
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 2.75e1
  variant carriers: 7466
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 9683
  bin: 2.25e1
  variant carriers: 5889
genotype quality: GenotypeQuality
num of homozygotes: 13815
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-65147295-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147295
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147295
    reference: chr 11
allele count: 1
allele frequency: 8.354079296920687e-6
allele num: 119702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*82+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.153+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*82+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-263G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*148+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2630G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*129+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.572+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.153+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-263G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.27+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*207+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.153+43G>T
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.27+43G>T
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12935
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

11-65147295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147295
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147295
    reference: chr 11
allele count: 3
allele frequency: 2.506223789076206e-5
allele num: 119702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*207+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.27+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.153+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-263G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2630G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*148+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.153+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*82+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*82+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-263G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.27+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.153+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.572+43G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*129+43G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11555
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12935
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

11-65147298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65147298
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65147298
    reference: chr 11
allele count: 2
allele frequency: 1.670201927413024e-5
allele num: 119746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000407530
  ensembl transcript: ENST00000417511
  gene symbol: SLC25A45
  hgvsc: ENST00000417511.2:c.27+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435547
  ensembl transcript: ENST00000526432
  gene symbol: SLC25A45
  hgvsc: ENST00000526432.1:c.153+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000294187
  ensembl transcript: ENST00000294187
  gene symbol: SLC25A45
  hgvsc: ENST00000294187.6:c.27+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431891
  ensembl transcript: ENST00000533629
  gene symbol: SLC25A45
  hgvsc: ENST00000533629.1:c.*82+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433693
  ensembl transcript: ENST00000524438
  gene symbol: SLC25A45
  hgvsc: ENST00000524438.1:c.*148+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000525944
  gene symbol: SLC25A45
  hgvsc: ENST00000525944.1:n.572+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000162241
  ensembl transcript: ENST00000531791
  gene symbol: SLC25A45
  hgvsc: ENST00000531791.1:n.2627G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000434582
  ensembl transcript: ENST00000526898
  gene symbol: SLC25A45
  hgvsc: ENST00000526898.1:c.*207+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000381782
  ensembl transcript: ENST00000398802
  gene symbol: SLC25A45
  hgvsc: ENST00000398802.1:c.153+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431642
  ensembl transcript: ENST00000530936
  gene symbol: SLC25A45
  hgvsc: ENST00000530936.1:c.153+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000366357
  ensembl transcript: ENST00000377152
  gene symbol: SLC25A45
  hgvsc: ENST00000377152.2:c.27+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000433729
  ensembl transcript: ENST00000526259
  gene symbol: SLC25A45
  hgvsc: ENST00000526259.1:c.*82+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435000
  ensembl transcript: ENST00000529962
  gene symbol: SLC25A45
  hgvsc: ENST00000529962.1:c.*129+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000353879
  ensembl transcript: ENST00000360662
  gene symbol: SLC25A45
  hgvsc: ENST00000360662.3:c.82-266G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000435489
  ensembl transcript: ENST00000527174
  gene symbol: SLC25A45
  hgvsc: ENST00000527174.1:c.153+40G>A
  variant of: http://identifiers.org/hgnc/27442
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000162241
  ensembl protein: ENSP00000431769
  ensembl transcript: ENST00000534028
  gene symbol: SLC25A45
  hgvsc: ENST00000534028.1:c.82-266G>A
  variant of: http://identifiers.org/hgnc/27442
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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European (Non-Finnish)
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Latino
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16186
num of homozygotes: 0

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

South Asian
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East Asian
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Other
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Latino
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European (Non-Finnish)
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65914
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.514554872323024e-5
allele num: 66026
num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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East Asian
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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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Latino
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 66070
num of homozygotes: 0

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.03950103950104e-4
allele num: 9620
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.537616843633724e-5
allele num: 66114
num of homozygotes: 0

MQRankSum
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SIO_000300: -5.1e-2

VQSLOD
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QD
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ClippingRankSum
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SIO_000300: -2.41e-1

FS
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MQ
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SIO_000300: 5.896e1

BaseQRankSum
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SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
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SIO_000300: 1.687232e6

ReadPosRankSum
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SIO_000300: 1.71e0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.084205402774397e-5
allele num: 16436
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.038637307852098e-4
allele num: 9628
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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DP
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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QD
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VQSLOD
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SIO_000300: 3.92e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66182
num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele frequency: 3.526922172584058e-4
allele num: 8506
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.688201e6

VQSLOD
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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MQRankSum
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SIO_000300: 2.6e-1

ReadPosRankSum
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SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.039e1

BaseQRankSum
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SIO_000300: -3.587e0

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511395925276585e-5
allele num: 66164
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.688942e6

MQ
type: SiteQuality
SIO_000300: 5.917e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

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

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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.359639846511769e-4
allele num: 66194
num of homozygotes: 0

East Asian
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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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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InbreedingCoeff
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SIO_000300: 3.2e-3

GenotypeDepth
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variant carriers: 2

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

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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num of homozygotes: 0

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

Other
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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European (Finnish)
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South Asian
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -4.202e0

MQ
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SIO_000300: 5.886e1

DP
type: SiteQuality
SIO_000300: 1.690267e6

FS
type: SiteQuality
SIO_000300: 1.0012e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 76

GenotypeDepth
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variant carriers: 97

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1094

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

Latino
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allele count: 39
allele frequency: 3.382480485689506e-3
allele num: 11530
num of homozygotes: 0

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

Other
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allele count: 3
allele frequency: 3.36322869955157e-3
allele num: 892
num of homozygotes: 0

African
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allele count: 1115
allele frequency: 1.149484536082474e-1
allele num: 9700
num of homozygotes: 62

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: 6
allele frequency: 3.642987249544627e-4
allele num: 16470
num of homozygotes: 1

European (Non-Finnish)
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allele count: 11
allele frequency: 1.659225292627006e-4
allele num: 66296
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.72e-1

BaseQRankSum
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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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InbreedingCoeff
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SIO_000300: 8.57e-2

DP
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SIO_000300: 1.713076e6

ReadPosRankSum
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SIO_000300: 3.27e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.17e0

DP
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SIO_000300: 1.679822e6

ClippingRankSum
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SIO_000300: -2.05e-1

BaseQRankSum
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QD
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VQSLOD
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SIO_000300: 6.39e-1

FS
type: SiteQuality
SIO_000300: 1.115e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9696
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.821493624772313e-4
allele num: 16470
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66278
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.0494e1

ReadPosRankSum
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: -9.836e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

DP
type: SiteQuality
SIO_000300: 1.679486e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 1
allele frequency: 1.172332942555686e-4
allele num: 8530
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.031353135313531e-4
allele num: 9696
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.017592564651921e-5
allele num: 66278
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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European (Finnish)
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African
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allele num: 9706
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Latino
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European (Non-Finnish)
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East Asian
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VQSLOD
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele 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: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

Latino
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European (Finnish)
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East Asian
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Other
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South Asian
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VQSLOD
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MQ
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DP
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
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

MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.2e-3

MQ
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SIO_000300: 5.968e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

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

East Asian
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allele frequency: 2.334267040149393e-4
allele num: 8568
num of homozygotes: 0

South Asian
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ClippingRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.011322572874006e-5
allele num: 66416
num of homozygotes: 0

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 5.22e-1

MQ
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SIO_000300: 5.745e1

ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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QD
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SIO_000300: 1.617e1

FS
type: SiteQuality
SIO_000300: 2.454e0

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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ClippingRankSum
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SIO_000300: -3.532e0

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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DP
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SIO_000300: 1.67292e6

MQ
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SIO_000300: 5.467e1

BaseQRankSum
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SIO_000300: 5.570000000000001e-1

QD
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SIO_000300: 1.684e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.525360464766262e-5
allele num: 66442
num of homozygotes: 0

Other
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Latino
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allele frequency: 0.0e0
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South Asian
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African
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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

East Asian
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BaseQRankSum
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SIO_000300: 8.93e-1

VQSLOD
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QD
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FS
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DP
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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SIO_000300: 5.906e1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

African
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Latino
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East Asian
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Other
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South Asian
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South 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: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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VQSLOD
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FS
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MQRankSum
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SIO_000300: -1.4e-2

ClippingRankSum
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QD
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SIO_000300: 2.504e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.004627125773691e-5
allele num: 66564
num of homozygotes: 0

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

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

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

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

VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 1.674697e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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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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African
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allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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DP
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SIO_000300: 1.675e6

ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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SIO_000300: 3.568e0

VQSLOD
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GenotypeDepth
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variant carriers: 0

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

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

South Asian
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allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

Other
type: Population
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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QD
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 47

Other
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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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South Asian
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allele frequency: 2.80214424951267e-3
allele num: 16416
num of homozygotes: 2

Latino
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allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
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European (Finnish)
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
type: Population
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.84e1

VQSLOD
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SIO_000300: -2.617e0

ReadPosRankSum
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SIO_000300: -1.98e-1

DP
type: SiteQuality
SIO_000300: 1.67408e6

QD
type: SiteQuality
SIO_000300: 2.51e0

FS
type: SiteQuality
SIO_000300: 5.012e0

MQRankSum
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SIO_000300: 1.51e0

BaseQRankSum
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SIO_000300: 2.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.55e-1

GenotypeDepth
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variant carriers: 0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66580
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

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

DP
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.977e1

FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -4.411e-1

QD
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SIO_000300: 1.119e1

MQRankSum
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SIO_000300: 1.7e-2

ClippingRankSum
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SIO_000300: -2.299e0

InbreedingCoeff
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SIO_000300: 2.0e-4

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 2
allele frequency: 1.235635734585444e-4
allele num: 16186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
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allele count: 8
allele frequency: 6.921612735767433e-4
allele num: 11558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

VQSLOD
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SIO_000300: 1.17e0

QD
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SIO_000300: 1.39e1

DP
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SIO_000300: 1.667427e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ReadPosRankSum
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SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 2.885e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507386192342478e-5
allele num: 66340
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
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
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SIO_000300: 1.660421e6

ReadPosRankSum
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SIO_000300: 4.08e-1

BaseQRankSum
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SIO_000300: 1.1e0

FS
type: SiteQuality
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MQRankSum
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QD
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MQ
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SIO_000300: 5.948e1

InbreedingCoeff
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SIO_000300: 2.0e-4

VQSLOD
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SIO_000300: 4.19e-1

ClippingRankSum
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SIO_000300: -5.600000000000001e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.287726358148894e-5
allele num: 15904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66284
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East Asian
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 9
allele frequency: 1.044325829658854e-3
allele num: 8618
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 1.79e0

FS
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 45
bin: 4.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66146
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.0275380189067e-4
allele num: 9732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.89e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.721e0

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

FS
type: SiteQuality
SIO_000300: 1.217e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: -7.785e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.529e0

DP
type: SiteQuality
SIO_000300: 1.649788e6

GenotypeDepth
all individuals: 71
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 130
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1655
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variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15540
num of homozygotes: 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: 1
allele frequency: 1.513500423780119e-5
allele num: 66072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

DP
type: SiteQuality
SIO_000300: 1.64599e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

FS
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.546e1

GenotypeDepth
all individuals: 30475
bin: 2.75e1
variant carriers: 10

GenotypeDepth
all individuals: 380
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 19
bin: 9.25e1
variant carriers: 9

GenotypeDepth
all individuals: 408
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variant carriers: 35

GenotypeDepth
all individuals: 254
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variant carriers: 46

GenotypeDepth
all individuals: 201
bin: 5.25e1
variant carriers: 51

GenotypeDepth
all individuals: 1161
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variant carriers: 0

GenotypeDepth
all individuals: 33
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variant carriers: 13

GenotypeDepth
all individuals: 1439
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variant carriers: 0

GenotypeDepth
all individuals: 59
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variant carriers: 10

GenotypeDepth
all individuals: 87
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variant carriers: 26

GenotypeDepth
all individuals: 23
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variant carriers: 6

GenotypeDepth
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variant carriers: 19

GenotypeQuality
all individuals: 261
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 385

GenotypeQuality
all individuals: 43298
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variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 284
allele frequency: 4.309429152377773e-3
allele num: 65902
num of homozygotes: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.313025210084034e-4
allele num: 15232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.219422249539029e-4
allele num: 6508
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.597701149425287e-3
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 27
allele frequency: 2.782931354359926e-3
allele num: 9702
num of homozygotes: 0

Latino
type: Population
allele count: 64
allele frequency: 5.562315313749349e-3
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

DP
type: SiteQuality
SIO_000300: 1.641058e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.011e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeDepth
all individuals: 27663
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 110
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variant carriers: 0

GenotypeDepth
all individuals: 60
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variant carriers: 0

GenotypeDepth
all individuals: 1555
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variant carriers: 0

GenotypeDepth
all individuals: 49
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variant carriers: 0

GenotypeDepth
all individuals: 10764
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variant carriers: 1

GenotypeDepth
all individuals: 202
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variant carriers: 0

GenotypeDepth
all individuals: 2766
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GenotypeDepth
all individuals: 151
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GenotypeDepth
all individuals: 17
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GenotypeDepth
all individuals: 339
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GenotypeDepth
all individuals: 29
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GenotypeDepth
all individuals: 17
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GenotypeDepth
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GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 314
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 390
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GenotypeQuality
all individuals: 610
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GenotypeQuality
all individuals: 39352
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6135
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variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64440
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.051303616484441e-4
allele num: 9512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.136e0

DP
type: SiteQuality
SIO_000300: 1.53568e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.115e1

MQ
type: SiteQuality
SIO_000300: 6.153e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 49
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
all individuals: 366
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.788835564536499e-4
allele num: 7918
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11682
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.082e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 1.261322e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 6.262e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-2

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeDepth
all individuals: 111
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 23972
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GenotypeQuality
all individuals: 1033
bin: 9.75e1
variant carriers: 38

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.333924499619965e-4
allele num: 7894
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.876318312559923e-4
allele num: 10430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 30
allele frequency: 4.943153732081067e-4
allele num: 60690
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

DP
type: SiteQuality
SIO_000300: 1.24152e6

QD
type: SiteQuality
SIO_000300: 1.417e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeDepth
all individuals: 2615
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variant carriers: 0

GenotypeDepth
all individuals: 49
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variant carriers: 0

GenotypeDepth
all individuals: 60
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variant carriers: 0

GenotypeDepth
all individuals: 10
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GenotypeDepth
all individuals: 12070
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GenotypeDepth
all individuals: 5407
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variant carriers: 2

GenotypeDepth
all individuals: 148
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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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 count: 0
allele frequency: 0.0e0
allele num: 710
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

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

African
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allele count: 3
allele frequency: 3.521953510213665e-4
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57400
num of homozygotes: 0

VQSLOD
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ReadPosRankSum
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FS
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QD
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MQRankSum
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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SIO_000300: -4.9e-3

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.493327744008943e-5
allele num: 57252
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -4.7e-3

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

Latino
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allele count: 3
allele frequency: 3.062474479379339e-4
allele num: 9796
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9792
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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7302
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57258
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: 8.76e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele count: 2
allele frequency: 2.998500749625187e-4
allele num: 6670
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53588
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -2.52e0

QD
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MQRankSum
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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VQSLOD
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SIO_000300: -3.646e-1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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: 1.514004542013626e-5
allele num: 66050
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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
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FS
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ClippingRankSum
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QD
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InbreedingCoeff
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SIO_000300: 1.85e-2

MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.812192e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

GenotypeDepth
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variant carriers: 1263

GenotypeDepth
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variant carriers: 2139

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 465

GenotypeQuality
all individuals: 36157
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variant carriers: 32330

European (Non-Finnish)
type: Population
allele count: 36781
allele frequency: 5.599177957071092e-1
allele num: 65690
num of homozygotes: 10254

African
type: Population
allele count: 1271
allele frequency: 1.340151834668916e-1
allele num: 9484
num of homozygotes: 89

European (Finnish)
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allele count: 3942
allele frequency: 6.123019571295434e-1
allele num: 6438
num of homozygotes: 1214

Latino
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allele count: 2729
allele frequency: 2.401865868685091e-1
allele num: 11362
num of homozygotes: 363

East Asian
type: Population
allele count: 2356
allele frequency: 2.765258215962441e-1
allele num: 8520
num of homozygotes: 332

South Asian
type: Population
allele count: 6797
allele frequency: 4.142996464708034e-1
allele num: 16406
num of homozygotes: 1450

Other
type: Population
allele count: 441
allele frequency: 5.080645161290323e-1
allele num: 868
num of homozygotes: 113

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.11e-2

ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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QD
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SIO_000300: 2.018e1

ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 1.940436e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.909e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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bin: 5.25e1
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GenotypeDepth
all individuals: 1025
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 863
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66294
num of homozygotes: 0

South Asian
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allele count: 1
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allele num: 16440
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.014e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.346e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.202e1

DP
type: SiteQuality
SIO_000300: 1.933623e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66294
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9512
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.824817518248175e-4
allele num: 16440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.346e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-2

QD
type: SiteQuality
SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 1.014e0

ClippingRankSum
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SIO_000300: -6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.933623e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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