http://identifiers.org/exac.variant/17-8192987-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8192987
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8192987
    reference: chr 17
allele count: 1
allele frequency: 8.415100055539661e-6
allele num: 118834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.861-26G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-144C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.861-26G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*108C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*61-26G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*61-26G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*77C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*61-26G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.437+81C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.512C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.861-26G>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-8192989-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8192989
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8192989
    reference: chr 17
allele count: 1
allele frequency: 8.416374899003501e-6
allele num: 118816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*110C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*61-28G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.437+83C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.861-28G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*61-28G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*61-28G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*79C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.514C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.861-28G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-142C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.861-28G>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-8192999-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8192999
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8192999
    reference: chr 17
allele count: 1
allele frequency: 8.4088730428348e-6
allele num: 118922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.861-38G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*120C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-132C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*61-38G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*61-38G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.524C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.861-38G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.437+93C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*89C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*61-38G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.861-38G>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS

17-8193001-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193001
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193001
    reference: chr 17
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*91T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*61-40A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.437+95T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.861-40A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.526T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.861-40A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*122T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-130T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*61-40A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.861-40A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*61-40A>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11455
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4820
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

17-8193002-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193002
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193002
    reference: chr 17
allele count: 1
allele frequency: 8.401384548173538e-6
allele num: 119028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*61-41G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*61-41G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.861-41G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*123C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.527C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*61-41G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.861-41G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*92C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.861-41G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.437+96C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-129C>T
  variant of: http://identifiers.org/hgnc/17679
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11448
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

17-8193005-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193005
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193005
    reference: chr 17
allele count: 27
allele frequency: 2.26627944064866e-4
allele num: 119138
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.437+99A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*61-44T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.861-44T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*95A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*126A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.530A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-126A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.861-44T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.861-44T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*61-44T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*61-44T>C
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11396
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14060
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

17-8193090-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193090
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193090
    reference: chr 17
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-41C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+82G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+82G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.615C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-41C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+82G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+82G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*211C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+82G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*180C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+82G>C
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

17-8193092-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193092
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193092
    reference: chr 17
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-39T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*182T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+80A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+80A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.617T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+80A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+80A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*213T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-39T>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+80A>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+80A>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

17-8193099-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193099
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193099
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-32T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.624T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*220T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+73A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+73A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+73A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+73A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+73A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*189T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-32T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+73A>G
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6795
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-8193105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193105
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193105
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+67C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+67C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+67C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*195G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*226G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-26G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.630G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+67C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+67C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-26G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+67C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-8193115-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193115
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193115
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+57C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.640G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*205G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-16G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+57C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+57C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*236G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+57C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+57C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-16G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+57C>G
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-8193119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193119
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193119
    reference: chr 17
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-12C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*240C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+53G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*209C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+53G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+53G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+53G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+53G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+53G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.644C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-12C>T
  variant of: http://identifiers.org/hgnc/17679
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

17-8193122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193122
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193122
    reference: chr 17
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*243C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-9C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+50G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-9C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+50G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+50G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.647C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+50G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*212C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+50G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+50G>A
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/17-8193126-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193126
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193126
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-5C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*216C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-5C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*247C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.651C>A
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.438-5C>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-8193127-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193127
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193127
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*248C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+45G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-4C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*217C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-4C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.652C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+45G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+45G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+45G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+45G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+45G>C
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6723
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.438-4C>G
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-8193129-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193129
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193129
    reference: chr 17
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+43T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*219A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.352-2A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.654A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+43T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+43T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*250A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+43T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+43T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.438-2A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+43T>G
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6835
  bin: 6.25e1
  variant carriers: 0
hgvs: c.438-2A>C
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-8193156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193156
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193156
    reference: chr 17
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+16G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.463C>T
  hgvsp: ENSP00000226105.6:p.Pro155Ser
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+16G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.681C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*246C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+16G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*277C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+16G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+16G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+16G>A
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro155Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

17-8193158-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193158
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193158
    reference: chr 17
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.683C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+14G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+14G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+14G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*248C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+14G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*279C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.465C>T
  hgvsp: ENST00000226105.6:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+14G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+14G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*22C>T
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro155Pro
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

17-8193159-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193159
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193159
    reference: chr 17
allele count: 16
allele frequency: 1.318044022670357e-4
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.466G>A
  hgvsp: ENSP00000226105.6:p.Glu156Lys
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+13C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*249G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+13C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.684G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+13C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*23G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+13C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*280G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+13C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+13C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu156Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

17-8193164-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193164
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193164
    reference: chr 17
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60+8A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.689T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*285T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860+8A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60+8A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860+8A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60+8A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.471T>G
  hgvsp: ENSP00000226105.6:p.Asn157Lys
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*254T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860+8A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*28T>G
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn157Lys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

17-8193172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193172
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193172
    reference: chr 17
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.860G>A
  hgvsp: ENSP00000369407.2:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*293C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*36C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*262C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.860G>A
  hgvsp: ENSP00000462395.1:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.479C>T
  hgvsp: ENSP00000226105.6:p.Pro160Leu
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.697C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.860G>A
  hgvsp: ENSP00000464071.1:p.Ser287Asn
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser287Asn
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

17-8193176-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193176
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193176
    reference: chr 17
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*40A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.701A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*56T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.856T>C
  hgvsp: ENSP00000462395.1:p.Cys286Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*297A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.856T>C
  hgvsp: ENSP00000464071.1:p.Cys286Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*266A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*56T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.856T>C
  hgvsp: ENSP00000369407.2:p.Cys286Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*56T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.483A>G
  hgvsp: ENST00000226105.6:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys286Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/17-8193186-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193186
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193186
    reference: chr 17
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*307C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.846G>T
  hgvsp: ENSP00000369407.2:p.Gln282His
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.846G>T
  hgvsp: ENSP00000462395.1:p.Gln282His
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*50C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*276C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*46G>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.846G>T
  hgvsp: ENSP00000464071.1:p.Gln282His
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.711C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.493C>A
  hgvsp: ENSP00000226105.6:p.Leu165Met
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*46G>T
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu165Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

17-8193186-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193186
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193186
    reference: chr 17
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.493C>T
  hgvsp: ENST00000226105.6:c.493C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.846G>A
  hgvsp: ENST00000579192.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.846G>A
  hgvsp: ENST00000380067.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*276C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.846G>A
  hgvsp: ENST00000580340.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.711C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*307C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu165Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP

17-8193189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193189
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193189
    reference: chr 17
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.496G>A
  hgvsp: ENSP00000226105.6:p.Gly166Ser
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*279G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.843C>T
  hgvsp: ENST00000580340.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*43C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.843C>T
  hgvsp: ENST00000579192.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.843C>T
  hgvsp: ENST00000380067.2:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*53G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*310G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.714G>A
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly166Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

17-8193203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193203
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193203
    reference: chr 17
allele count: 293
allele frequency: 2.414463708879953e-3
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.728G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*67G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.829C>T
  hgvsp: ENST00000580340.1:c.829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.510G>A
  hgvsp: ENST00000226105.6:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.829C>T
  hgvsp: ENST00000579192.1:c.829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.829C>T
  hgvsp: ENST00000380067.2:c.829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*293G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*324G>A
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6853
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 9.75e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gln170Gln
num of homozygotes: 2
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

17-8193205-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193205
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193205
    reference: chr 17
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*326T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.827A>G
  hgvsp: ENSP00000369407.2:p.Gln276Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.827A>G
  hgvsp: ENSP00000464071.1:p.Gln276Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*69T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.512T>C
  hgvsp: ENSP00000226105.6:p.Leu171Pro
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.730T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.827A>G
  hgvsp: ENSP00000462395.1:p.Gln276Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*295T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu171Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-8193206-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193206
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193206
    reference: chr 17
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*327G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.826C>T
  hgvsp: ENSP00000464071.1:p.Gln276Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*26C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.826C>T
  hgvsp: ENSP00000369407.2:p.Gln276Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.513G>A
  hgvsp: ENST00000226105.6:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.826C>T
  hgvsp: ENSP00000462395.1:p.Gln276Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.731G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*296G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*26C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*26C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln276Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

17-8193221-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193221
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193221
    reference: chr 17
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.746C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.528C>G
  hgvsp: ENST00000226105.6:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*311C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.811G>C
  hgvsp: ENSP00000369407.2:p.Gly271Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.811G>C
  hgvsp: ENSP00000464071.1:p.Gly271Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*85C>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.811G>C
  hgvsp: ENSP00000462395.1:p.Gly271Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*342C>G
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly271Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

17-8193227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193227
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193227
    reference: chr 17
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*317C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.805G>A
  hgvsp: ENSP00000464071.1:p.Val269Met
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*91C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.534C>T
  hgvsp: ENST00000226105.6:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*348C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.805G>A
  hgvsp: ENSP00000462395.1:p.Val269Met
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.805G>A
  hgvsp: ENSP00000369407.2:p.Val269Met
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*5G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*5G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.752C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*5G>A
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val269Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

17-8193228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193228
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193228
    reference: chr 17
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.804C>T
  hgvsp: ENST00000579192.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*318G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.535G>A
  hgvsp: ENSP00000226105.6:p.Asp179Asn
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.804C>T
  hgvsp: ENST00000580340.1:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.804C>T
  hgvsp: ENST00000380067.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*349G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.753G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp179Asn
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

17-8193228-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193228
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193228
    reference: chr 17
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*349G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.*4C>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.*4C>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.804C>A
  hgvsp: ENST00000580340.1:c.804C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.804C>A
  hgvsp: ENST00000579192.1:c.804C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*92G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*318G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.804C>A
  hgvsp: ENST00000380067.2:c.804C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.535G>T
  hgvsp: ENSP00000226105.6:p.Asp179Tyr
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.753G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.*4C>A
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp179Tyr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/17-8193234-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193234
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193234
    reference: chr 17
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.759A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.862T>G
  hgvsp: ENSP00000464307.1:p.Ter288GluextTer?
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.874T>G
  hgvsp: ENSP00000379574.1:p.Ter292GluextTer52
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.798T>G
  hgvsp: ENST00000579192.1:c.798T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.541A>C
  hgvsp: ENSP00000226105.6:p.Asn181His
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.798T>G
  hgvsp: ENST00000380067.2:c.798T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*355A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.874T>G
  hgvsp: ENSP00000464191.1:p.Ter292GluextTer56
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*324A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.798T>G
  hgvsp: ENST00000580340.1:c.798T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*98A>C
  variant of: http://identifiers.org/hgnc/17679
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter288GluextTer?
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

17-8193236-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193236
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193236
    reference: chr 17
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*100C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.872G>A
  hgvsp: ENSP00000464191.1:p.Cys291Tyr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.796G>A
  hgvsp: ENSP00000464071.1:p.Val266Ile
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.543C>T
  hgvsp: ENST00000226105.6:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.872G>A
  hgvsp: ENSP00000379574.1:p.Cys291Tyr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.796G>A
  hgvsp: ENSP00000369407.2:p.Val266Ile
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*357C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.860G>A
  hgvsp: ENSP00000464307.1:p.Cys287Tyr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.796G>A
  hgvsp: ENSP00000462395.1:p.Val266Ile
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*326C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.761C>T
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val266Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/17-8193239-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193239
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193239
    reference: chr 17
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*103C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.793G>T
  hgvsp: ENSP00000464071.1:p.Asp265Tyr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.764C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.546C>A
  hgvsp: ENST00000226105.6:c.546C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.869G>T
  hgvsp: ENSP00000464191.1:p.Arg290Ile
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.793G>T
  hgvsp: ENSP00000369407.2:p.Asp265Tyr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.793G>T
  hgvsp: ENSP00000462395.1:p.Asp265Tyr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*360C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.857G>T
  hgvsp: ENSP00000464307.1:p.Arg286Ile
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*329C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.869G>T
  hgvsp: ENSP00000379574.1:p.Arg290Ile
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp265Tyr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

17-8193241-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193241
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193241
    reference: chr 17
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*331T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.766T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.867A>G
  hgvsp: ENST00000585311.1:c.867A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.791A>G
  hgvsp: ENSP00000462395.1:p.Lys264Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*362T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.548T>C
  hgvsp: ENSP00000226105.6:p.Phe183Ser
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*105T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.791A>G
  hgvsp: ENSP00000369407.2:p.Lys264Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.855A>G
  hgvsp: ENST00000579681.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.791A>G
  hgvsp: ENSP00000464071.1:p.Lys264Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.867A>G
  hgvsp: ENST00000396278.1:c.867A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys264Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

17-8193244-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193244
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193244
    reference: chr 17
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.788C>A
  hgvsp: ENSP00000462395.1:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.864C>A
  hgvsp: ENSP00000379574.1:p.Asp288Glu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.769G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.864C>A
  hgvsp: ENSP00000464191.1:p.Asp288Glu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*365G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.852C>A
  hgvsp: ENSP00000464307.1:p.Asp284Glu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.551G>T
  hgvsp: ENSP00000226105.6:p.Gly184Val
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.788C>A
  hgvsp: ENSP00000369407.2:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*108G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*334G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.788C>A
  hgvsp: ENSP00000464071.1:p.Thr263Asn
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly184Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-8193245-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193245
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193245
    reference: chr 17
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.787A>G
  hgvsp: ENSP00000464071.1:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*366T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.552T>C
  hgvsp: ENST00000226105.6:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.787A>G
  hgvsp: ENSP00000369407.2:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*109T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*335T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.863A>G
  hgvsp: ENSP00000464191.1:p.Asp288Gly
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.770T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.851A>G
  hgvsp: ENSP00000464307.1:p.Asp284Gly
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.787A>G
  hgvsp: ENSP00000462395.1:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.863A>G
  hgvsp: ENSP00000379574.1:p.Asp288Gly
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr263Ala
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-8193248-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193248
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193248
    reference: chr 17
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.784G>T
  hgvsp: ENSP00000462395.1:p.Gly262Trp
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.848G>T
  hgvsp: ENSP00000464307.1:p.Gly283Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.860G>T
  hgvsp: ENSP00000379574.1:p.Gly287Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*112C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.784G>T
  hgvsp: ENSP00000369407.2:p.Gly262Trp
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*338C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.860G>T
  hgvsp: ENSP00000464191.1:p.Gly287Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*369C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.555C>A
  hgvsp: ENST00000226105.6:c.555C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.773C>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.784G>T
  hgvsp: ENSP00000464071.1:p.Gly262Trp
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly262Trp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

17-8193258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193258
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193258
    reference: chr 17
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*4C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.838G>A
  hgvsp: ENSP00000464307.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.850G>A
  hgvsp: ENSP00000464191.1:p.Ala284Thr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*348C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.774G>A
  hgvsp: ENST00000579192.1:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*379C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.850G>A
  hgvsp: ENSP00000379574.1:p.Ala284Thr
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.774G>A
  hgvsp: ENST00000380067.2:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.774G>A
  hgvsp: ENST00000580340.1:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*122C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.783C>T
  variant of: http://identifiers.org/hgnc/17679
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala280Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

17-8193259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193259
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193259
    reference: chr 17
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*5G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*123G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.773C>T
  hgvsp: ENSP00000462395.1:p.Ala258Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.837C>T
  hgvsp: ENST00000579681.1:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.849C>T
  hgvsp: ENST00000585311.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.773C>T
  hgvsp: ENSP00000369407.2:p.Ala258Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.773C>T
  hgvsp: ENSP00000464071.1:p.Ala258Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*349G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.849C>T
  hgvsp: ENST00000396278.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000108961
  ensembl transcript: ENST00000580777
  gene symbol: RANGRF
  hgvsc: ENST00000580777.1:n.784G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*380G>A
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala258Val
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

17-8193265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193265
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193265
    reference: chr 17
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*129G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.767C>T
  hgvsp: ENSP00000369407.2:p.Ala256Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.831C>T
  hgvsp: ENST00000579681.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.843C>T
  hgvsp: ENST00000585311.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*355G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.767C>T
  hgvsp: ENSP00000462395.1:p.Ala256Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.767C>T
  hgvsp: ENSP00000464071.1:p.Ala256Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*11G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.843C>T
  hgvsp: ENST00000396278.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*386G>A
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala256Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

17-8193270-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193270
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193270
    reference: chr 17
allele count: 3
allele frequency: 2.479338842975207e-5
allele num: 121000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.838C>A
  hgvsp: ENSP00000379574.1:p.Gln280Lys
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.762C>A
  hgvsp: ENSP00000462395.1:p.Cys254Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.762C>A
  hgvsp: ENSP00000369407.2:p.Cys254Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.826C>A
  hgvsp: ENSP00000464307.1:p.Gln276Lys
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*360G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*391G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*134G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*16G>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.838C>A
  hgvsp: ENSP00000464191.1:p.Gln280Lys
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.762C>A
  hgvsp: ENSP00000464071.1:p.Cys254Ter
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys254Ter
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

17-8193277-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193277
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193276
    reference: chr 17
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.830delA
  hgvsp: ENSP00000464191.1:p.Asn277ThrfsTer45
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.818delA
  hgvsp: ENSP00000464307.1:p.Asn273ThrfsTer45
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*143delT
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*400delT
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.830delA
  hgvsp: ENSP00000379574.1:p.Asn277ThrfsTer45
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*25delT
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.754delA
  hgvsp: ENSP00000464071.1:p.Thr252HisfsTer18
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.754delA
  hgvsp: ENSP00000369407.2:p.Thr252HisfsTer18
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*369delT
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.754delA
  hgvsp: ENSP00000462395.1:p.Thr252HisfsTer18
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr252HisfsTer18
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: GT
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

17-8193285-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193285
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193285
    reference: chr 17
allele count: 1
allele frequency: 8.276912380605539e-6
allele num: 120818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.811C>G
  hgvsp: ENSP00000464307.1:p.Leu271Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*149G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.823C>G
  hgvsp: ENSP00000464191.1:p.Leu275Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.747C>G
  hgvsp: ENSP00000464071.1:p.Phe249Leu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*31G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.747C>G
  hgvsp: ENSP00000462395.1:p.Phe249Leu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.747C>G
  hgvsp: ENSP00000369407.2:p.Phe249Leu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.823C>G
  hgvsp: ENSP00000379574.1:p.Leu275Val
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*375G>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*406G>C
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44043
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe249Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

17-8193289-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193289
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193289
    reference: chr 17
allele count: 3
allele frequency: 2.484554353767412e-5
allele num: 120746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.819A>G
  hgvsp: ENST00000585311.1:c.819A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.819A>G
  hgvsp: ENST00000396278.1:c.819A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*35T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.743A>G
  hgvsp: ENSP00000462395.1:p.Lys248Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.743A>G
  hgvsp: ENSP00000369407.2:p.Lys248Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.807A>G
  hgvsp: ENST00000579681.1:c.807A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.743A>G
  hgvsp: ENSP00000464071.1:p.Lys248Arg
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*153T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*379T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*410T>C
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys248Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

17-8193290-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193290
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193290
    reference: chr 17
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.742A>C
  hgvsp: ENSP00000369407.2:p.Lys248Gln
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.742A>C
  hgvsp: ENSP00000464071.1:p.Lys248Gln
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*36T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.742A>C
  hgvsp: ENSP00000462395.1:p.Lys248Gln
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.818A>C
  hgvsp: ENSP00000379574.1:p.Gln273Pro
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*380T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.806A>C
  hgvsp: ENSP00000464307.1:p.Gln269Pro
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*411T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*154T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.818A>C
  hgvsp: ENSP00000464191.1:p.Gln273Pro
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys248Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ

17-8193297-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193297
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193297
    reference: chr 17
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*387T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.811A>G
  hgvsp: ENSP00000464191.1:p.Ser271Gly
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.735A>G
  hgvsp: ENST00000380067.2:c.735A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.799A>G
  hgvsp: ENSP00000464307.1:p.Ser267Gly
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.735A>G
  hgvsp: ENST00000579192.1:c.735A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*418T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.811A>G
  hgvsp: ENSP00000379574.1:p.Ser271Gly
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*161T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*43T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.735A>G
  hgvsp: ENST00000580340.1:c.735A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser267Gly
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

17-8193298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193298
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193298
    reference: chr 17
allele count: 3
allele frequency: 2.489006886252385e-5
allele num: 120530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.810G>A
  hgvsp: ENST00000396278.1:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.798G>A
  hgvsp: ENST00000579681.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.734G>A
  hgvsp: ENSP00000462395.1:p.Arg245Gln
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*44C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*388C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*419C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.734G>A
  hgvsp: ENSP00000369407.2:p.Arg245Gln
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.734G>A
  hgvsp: ENSP00000464071.1:p.Arg245Gln
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*162C>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.810G>A
  hgvsp: ENST00000585311.1:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg245Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

17-8193299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193299
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193299
    reference: chr 17
allele count: 6
allele frequency: 4.980575754557227e-5
allele num: 120468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.797C>T
  hgvsp: ENSP00000464307.1:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.809C>T
  hgvsp: ENSP00000379574.1:p.Pro270Leu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.733C>T
  hgvsp: ENSP00000462395.1:p.Arg245Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.809C>T
  hgvsp: ENSP00000464191.1:p.Pro270Leu
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*163G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.733C>T
  hgvsp: ENSP00000369407.2:p.Arg245Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.733C>T
  hgvsp: ENSP00000464071.1:p.Arg245Ter
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*45G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*389G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*420G>A
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg245Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

17-8193304-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193304
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193304
    reference: chr 17
allele count: 2
allele frequency: 1.66118475696867e-5
allele num: 120396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*168T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-2A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-2A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-2A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-2A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-2A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*394T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-2A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*425T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*50T>G
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: c.730-2A>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

17-8193306-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193306
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193306
    reference: chr 17
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-4A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-4A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-4A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*170T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*427T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*52T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-4A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-4A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*396T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-4A>C
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 2.25e1
  variant carriers: 0
hgvs: c.730-4A>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

17-8193308-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193308
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193309
    reference: chr 17
allele count: 3
allele frequency: 2.493724127612176e-5
allele num: 120302
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-7dupC
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-7dupC
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*434dupG
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*177dupG
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-7dupC
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*59dupG
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-7dupC
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-7dupC
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-7dupC
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*403dupG
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: c.730-7dupC
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

17-8193314-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193314
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193314
    reference: chr 17
allele count: 1
allele frequency: 8.32639467110741e-6
allele num: 120100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*404A>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*60A>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-12T>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*435A>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-12T>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-12T>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*178A>T
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-12T>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-12T>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-12T>A
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

17-8193323-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193323
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193323
    reference: chr 17
allele count: 1
allele frequency: 8.349196807267141e-6
allele num: 119772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-21A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-21A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-21A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-21A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*187T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-21A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*69T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-21A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*444T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*413T>C
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/17-8193328-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193328
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193328
    reference: chr 17
allele count: 1
allele frequency: 8.356871855726965e-6
allele num: 119662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-26T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*74A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*449A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-26T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*418A>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-26T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-26T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-26T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-26T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*192A>C
  variant of: http://identifiers.org/hgnc/17679
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-8193328-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193328
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193328
    reference: chr 17
allele count: 3
allele frequency: 2.507061556718089e-5
allele num: 119662
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*74A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-26T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-26T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-26T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-26T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*449A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*192A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*418A>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-26T>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-26T>C
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-8193332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193332
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193332
    reference: chr 17
allele count: 1
allele frequency: 8.365960579593749e-6
allele num: 119532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-30C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-30C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*78G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-30C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-30C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*453G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-30C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*196G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*422G>A
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-30C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

17-8193341-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193341
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193341
    reference: chr 17
allele count: 1
allele frequency: 8.390106386548982e-6
allele num: 119188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*431T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-39A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-39A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*462T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-39A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-39A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*87T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-39A>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*205T>G
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-39A>C
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

17-8193353-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193353
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193353
    reference: chr 17
allele count: 1
allele frequency: 8.429002511842749e-6
allele num: 118638
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000226105
  ensembl transcript: ENST00000226105
  gene symbol: RANGRF
  hgvsc: ENST00000226105.6:c.*99T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.806-51A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.806-51A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.730-51A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000383940
  ensembl transcript: ENST00000407006
  gene symbol: RANGRF
  hgvsc: ENST00000407006.4:c.*443T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000413190
  ensembl transcript: ENST00000439238
  gene symbol: RANGRF
  hgvsc: ENST00000439238.3:c.*474T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.794-51A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000108961
  ensembl protein: ENSP00000462310
  ensembl transcript: ENST00000580434
  gene symbol: RANGRF
  hgvsc: ENST00000580434.1:c.*217T>C
  variant of: http://identifiers.org/hgnc/17679
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.730-51A>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.730-51A>G
  variant of: http://identifiers.org/hgnc/31921
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2138
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-8193785-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193785
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193785
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 10848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+148T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+375T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+136T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+375T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+136T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+375T>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.*38T>G
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

17-8193818-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193818
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193818
    reference: chr 17
allele count: 1
allele frequency: 7.782101167315176e-5
allele num: 12850
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+342C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.*5C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+115C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+103C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+342C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+103C>G
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+342C>G
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5903
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4208
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-8193819-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193819
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193819
    reference: chr 17
allele count: 2
allele frequency: 1.545117428924598e-4
allele num: 12944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+341C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+341C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+102C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+102C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+341C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+114C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

17-8193822-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193822
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193823
    reference: chr 17
allele count: 1
allele frequency: 7.613826709304096e-5
allele num: 13134
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+337dupA
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+110dupA
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+337dupA
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.903dupA
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+98dupA
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+98dupA
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+337dupA
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

17-8193851-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193851
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193851
    reference: chr 17
allele count: 2
allele frequency: 1.404297149276787e-4
allele num: 14242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+309G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.875G>C
  hgvsp: ENSP00000464231.1:p.Arg292Pro
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+309G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+82G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+70G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+70G>C
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+309G>C
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg292Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

17-8193894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193894
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193894
    reference: chr 17
allele count: 2
allele frequency: 1.34698275862069e-4
allele num: 14848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.832G>A
  hgvsp: ENSP00000464231.1:p.Gly278Ser
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+266G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+39G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+27G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+27G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+266G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+266G>A
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21434
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2967
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18457
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly278Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-8193899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193899
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193899
    reference: chr 17
allele count: 5
allele frequency: 3.357507386516251e-4
allele num: 14892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+261G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+261G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+261G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.805+22G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.805+22G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+34G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.827G>A
  hgvsp: ENSP00000464231.1:p.Arg276His
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5346
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Arg276His
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

17-8193925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193925
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193925
    reference: chr 17
allele count: 1
allele frequency: 6.490977541217708e-5
allele num: 15406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.801C>T
  hgvsp: ENST00000585311.1:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.801C>T
  hgvsp: ENST00000396278.1:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+235C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.793+8C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.801C>T
  hgvsp: ENST00000577745.1:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+235C>T
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+235C>T
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34337
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32092
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3864
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: c.793+8C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

17-8193941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8193941
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 8193941
    reference: chr 17
allele count: 47
allele frequency: 2.940440440440441e-3
allele num: 15984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464307
  ensembl transcript: ENST00000579681
  gene symbol: SLC25A35
  hgvsc: ENST00000579681.1:c.785G>A
  hgvsp: ENSP00000464307.1:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000379574
  ensembl transcript: ENST00000396278
  gene symbol: SLC25A35
  hgvsc: ENST00000396278.1:c.785G>A
  hgvsp: ENSP00000379574.1:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464071
  ensembl transcript: ENST00000580340
  gene symbol: SLC25A35
  hgvsc: ENST00000580340.1:c.729+219G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000369407
  ensembl transcript: ENST00000380067
  gene symbol: SLC25A35
  hgvsc: ENST00000380067.2:c.729+219G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000462395
  ensembl transcript: ENST00000579192
  gene symbol: SLC25A35
  hgvsc: ENST00000579192.1:c.729+219G>A
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464191
  ensembl transcript: ENST00000585311
  gene symbol: SLC25A35
  hgvsc: ENST00000585311.1:c.785G>A
  hgvsp: ENSP00000464191.1:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/31921
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125434
  ensembl protein: ENSP00000464231
  ensembl transcript: ENST00000577745
  gene symbol: SLC25A35
  hgvsc: ENST00000577745.1:c.785G>A
  hgvsp: ENSP00000464231.1:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/31921
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Gly262Asp
num of homozygotes: 1
reference allele: C

GenotypeQuality
all individuals: 4014
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4776
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18231
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3842
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10209
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2038
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7712
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517082347229808e-5
allele num: 65916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14912
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.89172e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.626e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

VQSLOD
type: SiteQuality
SIO_000300: -2.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 602
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10212
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3841
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517496737382015e-5
allele num: 65898
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

DP
type: SiteQuality
SIO_000300: 1.890196e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.045e0

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.692e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2564
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4806
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3982
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51758885482745e-5
allele num: 65894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-3

QD
type: SiteQuality
SIO_000300: 1.27e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.337e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

DP
type: SiteQuality
SIO_000300: 1.886034e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10219
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3984
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2568
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.612881893929374e-5
allele num: 15122
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

FS
type: SiteQuality
SIO_000300: 3.873e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
type: SiteQuality
SIO_000300: 1.8858e6

VQSLOD
type: SiteQuality
SIO_000300: -8.375e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.75e-1

QD
type: SiteQuality
SIO_000300: 1.812e1

GenotypeQuality
all individuals: 1394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16582
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4823
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1263
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7654
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10222
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 713
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3864
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3981
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.60763843002511e-5
allele num: 15134
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.041e0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.335e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 1.885816e6

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 1.698e1

GenotypeQuality
all individuals: 15342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3880
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variant carriers: 0

GenotypeQuality
all individuals: 1432
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variant carriers: 0

GenotypeQuality
all individuals: 1251
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 27

GenotypeQuality
all individuals: 7641
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variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 23
allele frequency: 2.660805182785748e-3
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.583278472679394e-5
allele num: 15190
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.900232018561485e-4
allele num: 10344
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 5.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

QD
type: SiteQuality
SIO_000300: 1.581e1

DP
type: SiteQuality
SIO_000300: 1.885902e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 967
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variant carriers: 0

GenotypeQuality
all individuals: 19
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.38e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: -1.156e0

FS
type: SiteQuality
SIO_000300: 6.729e0

QD
type: SiteQuality
SIO_000300: 1.274e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.164e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

DP
type: SiteQuality
SIO_000300: 3.212563e6

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 6754
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44083
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1702
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2268
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.884060757546626e-4
allele num: 10402
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.361e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.494e1

DP
type: SiteQuality
SIO_000300: 3.2127e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 1703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 44084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 2270
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 970
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1524
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 2151
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

QD
type: SiteQuality
SIO_000300: 1.63e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.269e0

DP
type: SiteQuality
SIO_000300: 3.213096e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

GenotypeQuality
all individuals: 44084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2271
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 1525
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.581e0

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.168e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.359e0

DP
type: SiteQuality
SIO_000300: 3.213304e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

GenotypeQuality
all individuals: 2152
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.398e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.626e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 3.213555e6

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
all individuals: 968
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variant carriers: 0

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

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

African
type: Population
allele count: 5
allele frequency: 4.805843906189927e-4
allele num: 10404
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
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MQ
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DP
type: SiteQuality
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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Latino
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FS
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SIO_000300: 9.72e-1

MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66738
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African
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Latino
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European (Finnish)
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South Asian
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FS
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Latino
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European (Finnish)
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South Asian
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Other
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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European (Non-Finnish)
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allele num: 66738
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South Asian
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Other
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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VQSLOD
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QD
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16510
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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allele num: 11576
num of homozygotes: 0

African
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East Asian
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Other
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European (Non-Finnish)
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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allele num: 66736
num of homozygotes: 0

Latino
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South Asian
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East Asian
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 9.619084263178146e-5
allele num: 10396
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VQSLOD
type: SiteQuality
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -2.716e0

GenotypeDepth
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variant carriers: 0

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele 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 frequency: 9.617234083477592e-5
allele num: 10398
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQ
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FS
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QD
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BaseQRankSum
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SIO_000300: -4.831e0

DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66722
num of homozygotes: 0

East Asian
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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allele num: 8652
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

DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.61e-1

MQ
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SIO_000300: 5.893e1

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11574
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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Other
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BaseQRankSum
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FS
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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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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GenotypeQuality
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South Asian
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allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66712
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European (Finnish)
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allele num: 6614
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East Asian
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African
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Latino
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Other
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FS
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
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allele num: 6614
num of homozygotes: 0

Other
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Latino
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African
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European (Non-Finnish)
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allele num: 66712
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East Asian
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South Asian
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QD
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.697e0

MQ
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SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 5.45e-1

ClippingRankSum
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SIO_000300: -7.9e-1

ReadPosRankSum
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SIO_000300: 6.21e-1

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

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

Latino
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allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66710
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Other
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allele frequency: 0.0e0
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African
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South Asian
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MQ
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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African
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allele num: 10380
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East Asian
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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Other
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European (Non-Finnish)
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African
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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FS
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 908
num of homozygotes: 0

African
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Latino
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South Asian
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European (Non-Finnish)
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allele num: 66694
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East 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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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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QD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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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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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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African
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South Asian
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Latino
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East Asian
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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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 (Non-Finnish)
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allele num: 66686
num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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Other
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

Other
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Latino
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num of homozygotes: 0

East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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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 frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
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European (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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East Asian
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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QD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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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 frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66634
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Latino
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South Asian
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African
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European (Finnish)
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Other
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DP
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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MQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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SIO_000300: -1.447e0

ReadPosRankSum
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SIO_000300: 1.96e0

DP
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 2.928543537680593e-4
allele num: 10244
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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 count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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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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QD
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DP
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Latino
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allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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SIO_000300: -1.639e0

DP
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SIO_000300: 3.205525e6

FS
type: SiteQuality
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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SIO_000300: 6.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

VQSLOD
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SIO_000300: 6.66e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

ReadPosRankSum
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SIO_000300: 1.21e0

QD
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VQSLOD
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MQ
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SIO_000300: 5.943e1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
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ClippingRankSum
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SIO_000300: -4.23e-1

FS
type: SiteQuality
SIO_000300: 4.145e0

BaseQRankSum
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SIO_000300: 3.24e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

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

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

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

Latino
type: Population
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allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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SIO_000300: 6.860000000000001e-1

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

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

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

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

African
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

BaseQRankSum
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DP
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66440
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 1.505434618974498e-5
allele num: 66426
num of homozygotes: 0

Other
type: Population
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Latino
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East Asian
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European (Finnish)
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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MQ
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.528986598403855e-5
allele num: 66410
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.945e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 3.198477e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.492e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013409673045051e-5
allele num: 66370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.137e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 3.196734e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 1.068e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.46e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

QD
type: SiteQuality
SIO_000300: 1.521e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.109481915933529e-5
allele num: 16368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

DP
type: SiteQuality
SIO_000300: 3.195663e6

QD
type: SiteQuality
SIO_000300: 1.297e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44034
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

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

African
type: Population
allele count: 3
allele frequency: 3.015075376884422e-4
allele num: 9950
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 1.032e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

FS
type: SiteQuality
SIO_000300: 1.877e0

MQ
type: SiteQuality
SIO_000300: 6.057e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

DP
type: SiteQuality
SIO_000300: 3.194175e6

GenotypeQuality
all individuals: 2007
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 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
all individuals: 21
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GenotypeQuality
all individuals: 1470
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.131207847946045e-5
allele num: 16310
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66242
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.615e0

VQSLOD
type: SiteQuality
SIO_000300: -8.055e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

DP
type: SiteQuality
SIO_000300: 3.188938e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66144
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.176645e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

QD
type: SiteQuality
SIO_000300: 1.031e1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513134003147319e-5
allele num: 66088
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

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

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.605523710265763e-4
allele num: 11514
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.85e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514325519413653e-5
allele num: 66036
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65908
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.255473539346929e-5
allele num: 15986
num of homozygotes: 0

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

South Asian
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allele frequency: 6.38895987733197e-5
allele num: 15652
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65768
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
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SIO_000300: 5.951e1

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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Latino
type: Population
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3228
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.329000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.395e1

QD
type: SiteQuality
SIO_000300: 1.099e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.39794e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.704164413196323e-4
allele num: 3698
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

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

FS
type: SiteQuality
SIO_000300: 7.89e-1

ReadPosRankSum
type: SiteQuality
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MQ
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

InbreedingCoeff
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SIO_000300: -5.59e-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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3726
num of homozygotes: 0

South Asian
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allele frequency: 2.710027100271003e-4
allele num: 7380
num of homozygotes: 0

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

QD
type: SiteQuality
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 7440
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 3776
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Latino
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Other
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African
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Non-Finnish)
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num of homozygotes: 0

African
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European (Finnish)
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East Asian
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Other
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BaseQRankSum
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 4352
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African
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Latino
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ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 192
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.551362683438155e-4
allele num: 7632
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

FS
type: SiteQuality
SIO_000300: 5.152e0

QD
type: SiteQuality
SIO_000300: 8.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.51909e5

VQSLOD
type: SiteQuality
SIO_000300: -1.404e0

GenotypeQuality
all individuals: 2086
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 696
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.300390117035111e-4
allele num: 7690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.932e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.99e-2

FS
type: SiteQuality
SIO_000300: 1.011e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 3.0267e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 5.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1