17-79682481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682481
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682481
    reference: chr 17
allele count: 9
allele frequency: 7.605590954417158e-5
allele num: 118334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.56-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.679-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.85-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.214-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.113-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*339-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.679-27C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.214-27C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28817
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

17-79682485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682485
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682485
    reference: chr 17
allele count: 4
allele frequency: 3.375242595561556e-5
allele num: 118510
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.679-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*339-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.85-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.56-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.214-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.679-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.214-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.113-23C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28817
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5246
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

17-79682496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682496
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682496
    reference: chr 17
allele count: 1
allele frequency: 8.393627557957998e-6
allele num: 119138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.214-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.56-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.85-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.214-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.679-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.113-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.679-12C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*339-12C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28817
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/17-79682502-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682502
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682502
    reference: chr 17
allele count: 15
allele frequency: 1.256176199648271e-4
allele num: 119410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.85-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.113-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.214-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.679-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.56-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.679-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.214-6C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*339-6C>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28818
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
hgvs: c.679-6C>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

17-79682504-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682504
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682504
    reference: chr 17
allele count: 3
allele frequency: 2.510502267820382e-5
allele num: 119498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.85-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*339-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.214-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.679-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.56-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.679-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.113-4C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.214-4C>G
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28815
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46261
  bin: 9.75e1
  variant carriers: 3
hgvs: c.679-4C>G
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

17-79682526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682526
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682526
    reference: chr 17
allele count: 4
allele frequency: 3.332555736994701e-5
allele num: 120028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.232C>T
  hgvsp: ENSP00000345580.5:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.697C>T
  hgvsp: ENSP00000461324.1:p.Arg233Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.131C>T
  hgvsp: ENSP00000458785.1:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.232C>T
  hgvsp: ENSP00000328403.5:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*357C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.74C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.103C>T
  hgvsp: ENSP00000446242.1:p.Arg35Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.697C>T
  hgvsp: ENSP00000439565.1:p.Arg233Trp
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28815
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg78Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

17-79682531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682531
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682531
    reference: chr 17
allele count: 117
allele frequency: 9.73928678453701e-4
allele num: 120132
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.237C>T
  hgvsp: ENST00000331531.5:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.702C>T
  hgvsp: ENST00000541223.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.702C>T
  hgvsp: ENST00000571730.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.79C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.136C>T
  hgvsp: ENST00000574884.1:c.136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.237C>T
  hgvsp: ENST00000350690.5:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.108C>T
  hgvsp: ENST00000545862.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*362C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28830
  bin: 9.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe79Phe
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

17-79682532-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682532
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682532
    reference: chr 17
allele count: 2
allele frequency: 1.664752201634787e-5
allele num: 120138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.238G>C
  hgvsp: ENSP00000345580.5:p.Ala80Pro
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.703G>C
  hgvsp: ENSP00000461324.1:p.Ala235Pro
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.109G>C
  hgvsp: ENSP00000446242.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.238G>C
  hgvsp: ENSP00000328403.5:p.Ala80Pro
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.137G>C
  hgvsp: ENSP00000458785.1:p.Ala47Pro
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.80G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.703G>C
  hgvsp: ENSP00000439565.1:p.Ala235Pro
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*363G>C
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28830
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala80Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

17-79682539-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682539
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682539
    reference: chr 17
allele count: 1
allele frequency: 8.317806760713336e-6
allele num: 120224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.710A>G
  hgvsp: ENSP00000439565.1:p.Tyr237Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.245A>G
  hgvsp: ENSP00000328403.5:p.Tyr82Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.144A>G
  hgvsp: ENSP00000458785.1:p.Tyr49Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.116A>G
  hgvsp: ENSP00000446242.1:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.710A>G
  hgvsp: ENSP00000461324.1:p.Tyr237Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.87A>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.245A>G
  hgvsp: ENSP00000345580.5:p.Tyr82Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*370A>G
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28830
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr82Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-79682540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682540
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682540
    reference: chr 17
allele count: 5
allele frequency: 4.158626655133409e-5
allele num: 120232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.117C>T
  hgvsp: ENST00000545862.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.711C>T
  hgvsp: ENST00000541223.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.145C>T
  hgvsp: ENST00000574884.1:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*371C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.711C>T
  hgvsp: ENST00000571730.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.246C>T
  hgvsp: ENST00000350690.5:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.88C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.246C>T
  hgvsp: ENST00000331531.5:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28831
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr82Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

17-79682550-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682550
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682550
    reference: chr 17
allele count: 8
allele frequency: 6.650373252198779e-5
allele num: 120294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.256C>T
  hgvsp: ENSP00000345580.5:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.155C>T
  hgvsp: ENSP00000458785.1:p.Arg53Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*381C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.98C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.256C>T
  hgvsp: ENSP00000328403.5:p.Arg86Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.721C>T
  hgvsp: ENSP00000439565.1:p.Arg241Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.127C>T
  hgvsp: ENSP00000446242.1:p.Arg43Trp
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.721C>T
  hgvsp: ENSP00000461324.1:p.Arg241Trp
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28828
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46317
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg86Trp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-79682551-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682551
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682551
    reference: chr 17
allele count: 2
allele frequency: 1.662095902933599e-5
allele num: 120330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.128G>A
  hgvsp: ENSP00000446242.1:p.Arg43Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.156G>A
  hgvsp: ENSP00000458785.1:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.722G>A
  hgvsp: ENSP00000439565.1:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.257G>A
  hgvsp: ENSP00000328403.5:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.722G>A
  hgvsp: ENSP00000461324.1:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*382G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.99G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.257G>A
  hgvsp: ENSP00000345580.5:p.Arg86Gln
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28826
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5888
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg86Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

17-79682553-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682553
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682553
    reference: chr 17
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.259G>T
  hgvsp: ENSP00000345580.5:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.724G>T
  hgvsp: ENSP00000461324.1:p.Asp242Tyr
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.158G>T
  hgvsp: ENSP00000458785.1:p.Asp54Tyr
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.724G>T
  hgvsp: ENSP00000439565.1:p.Asp242Tyr
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.130G>T
  hgvsp: ENSP00000446242.1:p.Asp44Tyr
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.259G>T
  hgvsp: ENSP00000328403.5:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.101G>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*384G>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28826
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46321
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp87Tyr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-79682556-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682556
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682556
    reference: chr 17
allele count: 4
allele frequency: 3.322921512593873e-5
allele num: 120376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.262C>T
  hgvsp: ENSP00000328403.5:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.727C>T
  hgvsp: ENSP00000439565.1:p.Arg243Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.262C>T
  hgvsp: ENSP00000345580.5:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.133C>T
  hgvsp: ENSP00000446242.1:p.Arg45Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*387C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.161C>T
  hgvsp: ENSP00000458785.1:p.Arg55Cys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.104C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.727C>T
  hgvsp: ENSP00000461324.1:p.Arg243Cys
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28825
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg88Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

17-79682557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682557
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682557
    reference: chr 17
allele count: 7
allele frequency: 5.814533009934545e-5
allele num: 120388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*388G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.105G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.263G>A
  hgvsp: ENSP00000345580.5:p.Arg88His
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.728G>A
  hgvsp: ENSP00000461324.1:p.Arg243His
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.162G>A
  hgvsp: ENSP00000458785.1:p.Arg55His
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.134G>A
  hgvsp: ENSP00000446242.1:p.Arg45His
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.263G>A
  hgvsp: ENSP00000328403.5:p.Arg88His
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.728G>A
  hgvsp: ENSP00000439565.1:p.Arg243His
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28826
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg88His
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

17-79682558-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682558
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682558
    reference: chr 17
allele count: 48052
allele frequency: 3.982099941990553e-1
allele num: 120670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*389T>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.135T>C
  hgvsp: ENST00000545862.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.264T>C
  hgvsp: ENST00000350690.5:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.163T>C
  hgvsp: ENST00000574884.1:c.163T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.264T>C
  hgvsp: ENST00000331531.5:c.264T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.729T>C
  hgvsp: ENST00000541223.1:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.106T>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.729T>C
  hgvsp: ENST00000571730.1:c.729T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 7.25e1
  variant carriers: 440
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.25e1
  variant carriers: 367
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 3.25e1
  variant carriers: 297
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 2.25e1
  variant carriers: 316
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 8.75e1
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 7.75e1
  variant carriers: 414
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 6.25e1
  variant carriers: 449
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 4.75e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.75e1
  variant carriers: 326
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 5.75e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 4.25e1
  variant carriers: 343
genotype depth: GenotypeDepth
  all individuals: 33163
  bin: 9.75e1
  variant carriers: 32352
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 431
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 324
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.25e1
  variant carriers: 381
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 7.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 7.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 19
hgvs: p.Arg88Arg
num of homozygotes: 9759
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

17-79682559-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682559
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682559
    reference: chr 17
allele count: 18
allele frequency: 1.492908683752177e-4
allele num: 120570
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.730G>A
  hgvsp: ENSP00000461324.1:p.Val244Met
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.107G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.730G>A
  hgvsp: ENSP00000439565.1:p.Val244Met
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.265G>A
  hgvsp: ENSP00000328403.5:p.Val89Met
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.265G>A
  hgvsp: ENSP00000345580.5:p.Val89Met
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.164G>A
  hgvsp: ENSP00000458785.1:p.Val56Met
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.136G>A
  hgvsp: ENSP00000446242.1:p.Val46Met
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*390G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44318
  bin: 9.75e1
  variant carriers: 18
hgvs: p.Val89Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

17-79682564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682564
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682564
    reference: chr 17
allele count: 2
allele frequency: 1.659145208388638e-5
allele num: 120544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.735C>T
  hgvsp: ENST00000541223.1:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.270C>T
  hgvsp: ENST00000331531.5:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.112C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*395C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.169C>T
  hgvsp: ENST00000574884.1:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.735C>T
  hgvsp: ENST00000571730.1:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.141C>T
  hgvsp: ENST00000545862.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.270C>T
  hgvsp: ENST00000350690.5:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11633
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala90Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

17-79682570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682570
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682570
    reference: chr 17
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.741C>T
  hgvsp: ENST00000541223.1:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.147C>T
  hgvsp: ENST00000545862.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.741C>T
  hgvsp: ENST00000571730.1:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.276C>T
  hgvsp: ENST00000331531.5:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.118C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.175C>T
  hgvsp: ENST00000574884.1:c.175C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.276C>T
  hgvsp: ENST00000350690.5:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*401C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly92Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

17-79682573-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682573
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682573
    reference: chr 17
allele count: 5
allele frequency: 4.14868901427149e-5
allele num: 120520
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.744C>G
  hgvsp: ENSP00000461324.1:p.Ser248Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.744C>G
  hgvsp: ENSP00000439565.1:p.Ser248Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.150C>G
  hgvsp: ENSP00000446242.1:p.Ser50Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.279C>G
  hgvsp: ENSP00000345580.5:p.Ser93Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.121C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.279C>G
  hgvsp: ENSP00000328403.5:p.Ser93Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.178C>G
  hgvsp: ENSP00000458785.1:p.Ser60Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*404C>G
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11632
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser93Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

17-79682579-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682579
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682578
    reference: chr 17
allele count: 12
allele frequency: 9.959498041298719e-5
allele num: 120488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.129delC
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*412delC
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.752delC
  hgvsp: ENSP00000439565.1:p.Pro251LeufsTer16
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.752delC
  hgvsp: ENSP00000461324.1:p.Pro251LeufsTer16
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.158delC
  hgvsp: ENSP00000446242.1:p.Pro53LeufsTer16
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.287delC
  hgvsp: ENSP00000328403.5:p.Pro96LeufsTer16
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.287delC
  hgvsp: ENSP00000345580.5:p.Pro96LeufsTer16
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.186delC
  hgvsp: ENSP00000458785.1:p.Pro63LeufsTer16
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11631
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro96LeufsTer16
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: GC
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-79682580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682580
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682580
    reference: chr 17
allele count: 1
allele frequency: 8.304820117596252e-6
allele num: 120412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.286C>T
  hgvsp: ENSP00000345580.5:p.Pro96Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.286C>T
  hgvsp: ENSP00000328403.5:p.Pro96Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.751C>T
  hgvsp: ENSP00000461324.1:p.Pro251Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.128C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.751C>T
  hgvsp: ENSP00000439565.1:p.Pro251Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.157C>T
  hgvsp: ENSP00000446242.1:p.Pro53Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*411C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.185C>T
  hgvsp: ENSP00000458785.1:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro96Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

17-79682581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682581
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682581
    reference: chr 17
allele count: 2
allele frequency: 1.660908849322349e-5
allele num: 120416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.186C>T
  hgvsp: ENSP00000458785.1:p.Pro63Leu
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.158C>T
  hgvsp: ENSP00000446242.1:p.Pro53Leu
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.752C>T
  hgvsp: ENSP00000461324.1:p.Pro251Leu
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.287C>T
  hgvsp: ENSP00000345580.5:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.287C>T
  hgvsp: ENSP00000328403.5:p.Pro96Leu
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.752C>T
  hgvsp: ENSP00000439565.1:p.Pro251Leu
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*412C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.129C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44291
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Pro96Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

17-79682590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682590
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682590
    reference: chr 17
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*421T>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.761T>C
  hgvsp: ENSP00000461324.1:p.Phe254Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.195T>C
  hgvsp: ENSP00000458785.1:p.Phe66Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.296T>C
  hgvsp: ENSP00000345580.5:p.Phe99Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.167T>C
  hgvsp: ENSP00000446242.1:p.Phe56Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.296T>C
  hgvsp: ENSP00000328403.5:p.Phe99Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.761T>C
  hgvsp: ENSP00000439565.1:p.Phe254Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.138T>C
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe99Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-79682594-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682594
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682594
    reference: chr 17
allele count: 3
allele frequency: 2.493268175925002e-5
allele num: 120324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.765C>G
  hgvsp: ENSP00000439565.1:p.His255Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.300C>G
  hgvsp: ENSP00000328403.5:p.His100Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*425C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.142C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.199C>G
  hgvsp: ENSP00000458785.1:p.His67Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.171C>G
  hgvsp: ENSP00000446242.1:p.His57Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.300C>G
  hgvsp: ENSP00000345580.5:p.His100Gln
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.765C>G
  hgvsp: ENSP00000461324.1:p.His255Gln
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 44294
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His100Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

17-79682595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682595
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682595
    reference: chr 17
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.301G>A
  hgvsp: ENSP00000328403.5:p.Glu101Lys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.200G>A
  hgvsp: ENSP00000458785.1:p.Glu68Lys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.766G>A
  hgvsp: ENSP00000439565.1:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.766G>A
  hgvsp: ENSP00000461324.1:p.Glu256Lys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*426G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.143G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.172G>A
  hgvsp: ENSP00000446242.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.301G>A
  hgvsp: ENSP00000345580.5:p.Glu101Lys
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu101Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

17-79682614-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682614
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682614
    reference: chr 17
allele count: 4
allele frequency: 3.332611267558696e-5
allele num: 120026
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.785C>T
  hgvsp: ENSP00000461324.1:p.Ser262Phe
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.785C>T
  hgvsp: ENSP00000439565.1:p.Ser262Phe
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.320C>T
  hgvsp: ENSP00000328403.5:p.Ser107Phe
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.320C>T
  hgvsp: ENSP00000345580.5:p.Ser107Phe
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.219C>T
  hgvsp: ENSP00000458785.1:p.Ser74Phe
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*445C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.191C>T
  hgvsp: ENSP00000446242.1:p.Ser64Phe
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.162C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11612
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44285
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Ser107Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-79682615-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682615
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682615
    reference: chr 17
allele count: 1
allele frequency: 8.334305668994715e-6
allele num: 119986
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.321C>A
  hgvsp: ENST00000331531.5:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*446C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.192C>A
  hgvsp: ENST00000545862.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.163C>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.220C>A
  hgvsp: ENST00000574884.1:c.220C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.786C>A
  hgvsp: ENST00000571730.1:c.786C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.321C>A
  hgvsp: ENST00000350690.5:c.321C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.786C>A
  hgvsp: ENST00000541223.1:c.786C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44287
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser107Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-79682615-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682615
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682615
    reference: chr 17
allele count: 8
allele frequency: 6.667444535195772e-5
allele num: 119986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*446C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.220C>T
  hgvsp: ENST00000574884.1:c.220C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.321C>T
  hgvsp: ENST00000350690.5:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.321C>T
  hgvsp: ENST00000331531.5:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.192C>T
  hgvsp: ENST00000545862.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.163C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.786C>T
  hgvsp: ENST00000541223.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.786C>T
  hgvsp: ENST00000571730.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser107Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

17-79682616-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682616
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682616
    reference: chr 17
allele count: 4
allele frequency: 3.334722801167153e-5
allele num: 119950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.221G>A
  hgvsp: ENSP00000458785.1:p.Val75Ile
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*447G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.787G>A
  hgvsp: ENSP00000439565.1:p.Val263Ile
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.322G>A
  hgvsp: ENSP00000328403.5:p.Val108Ile
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.193G>A
  hgvsp: ENSP00000446242.1:p.Val65Ile
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.164G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.322G>A
  hgvsp: ENSP00000345580.5:p.Val108Ile
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.787G>A
  hgvsp: ENSP00000461324.1:p.Val263Ile
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11603
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44283
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4965
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val108Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

17-79682621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682621
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682621
    reference: chr 17
allele count: 1
allele frequency: 8.349196807267141e-6
allele num: 119772
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.327C>T
  hgvsp: ENST00000331531.5:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.169C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.792C>T
  hgvsp: ENST00000571730.1:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.792C>T
  hgvsp: ENST00000541223.1:c.792C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.327C>T
  hgvsp: ENST00000350690.5:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.198C>T
  hgvsp: ENST00000545862.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*452C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.226C>T
  hgvsp: ENST00000574884.1:c.226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11603
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.25e1
  variant carriers: 0
hgvs: c.792C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

17-79682632-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682632
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682632
    reference: chr 17
allele count: 4
allele frequency: 3.352948079598987e-5
allele num: 119298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+10C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+10C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11602
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

17-79682633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682633
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682633
    reference: chr 17
allele count: 12
allele frequency: 1.006846556584777e-4
allele num: 119184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+11G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+11G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum

17-79682635-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682635
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682635
    reference: chr 17
allele count: 1
allele frequency: 8.385322331790435e-6
allele num: 119256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+13G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+13G>C
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11590
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

17-79682636-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682636
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682637
    reference: chr 17
allele count: 1
allele frequency: 8.390247176681825e-6
allele num: 119186
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+17dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+17dupG
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-79682636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682636
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682636
    reference: chr 17
allele count: 2
allele frequency: 1.678049435336365e-5
allele num: 119186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+14C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+14C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4504
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44268
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

17-79682637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682637
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682637
    reference: chr 17
allele count: 1
allele frequency: 8.395036854211791e-6
allele num: 119118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+15G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+15G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

17-79682640-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682640
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682641
    reference: chr 17
allele count: 1
allele frequency: 8.391796180054379e-6
allele num: 119164
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+23dupG
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+23dupG
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1936
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-79682641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682641
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682641
    reference: chr 17
allele count: 4
allele frequency: 3.354128932716174e-5
allele num: 119256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+19G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+19G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1658
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

17-79682643-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682643
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682643
    reference: chr 17
allele count: 1
allele frequency: 8.387291575804341e-6
allele num: 119228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+21G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+21G>C
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

17-79682649-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682649
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682649
    reference: chr 17
allele count: 2
allele frequency: 1.676670802454646e-5
allele num: 119284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+27G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+27G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4717
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

17-79682650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682650
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682650
    reference: chr 17
allele count: 14148
allele frequency: 1.185023871346009e-1
allele num: 119390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+28G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+28G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 5.75e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 6.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 2.25e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.25e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 8.75e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 8.25e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 5.25e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 7.25e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 4.25e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 3.75e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 7.75e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 2.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 6.25e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 11666
  bin: 9.75e1
  variant carriers: 10086
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.25e1
  variant carriers: 146
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 7.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 2.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 11
num of homozygotes: 1004
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-79682651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682651
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682651
    reference: chr 17
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+29C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42209
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

17-79682652-GCGGGGTGGTCAGGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682652
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682638
    reference: chr 17
allele count: 1
allele frequency: 8.377594960038872e-6
allele num: 119366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5392
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: GCGGGGTGGTCAGGT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

17-79682653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682653
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682653
    reference: chr 17
allele count: 4
allele frequency: 3.351543385729128e-5
allele num: 119348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+31C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5430
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-79682654-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682654
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682654
    reference: chr 17
allele count: 25
allele frequency: 2.092715675277494e-4
allele num: 119462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+32G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+32G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

17-79682659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682659
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682659
    reference: chr 17
allele count: 8
allele frequency: 6.688292144600876e-5
allele num: 119612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+37G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+37G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42204
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

17-79682662-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682662
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682662
    reference: chr 17
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+40C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+40C>G
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

17-79682665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682665
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682665
    reference: chr 17
allele count: 84
allele frequency: 7.01613711536534e-4
allele num: 119724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+43G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+43G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 9.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2272
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42216
  bin: 9.75e1
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-79682667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682667
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682667
    reference: chr 17
allele count: 4
allele frequency: 3.340236488743403e-5
allele num: 119752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+45C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+45C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42196
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

17-79682668-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682668
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682668
    reference: chr 17
allele count: 1
allele frequency: 8.348081610845828e-6
allele num: 119788
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+46G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+46G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5857
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

17-79682672-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682672
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682672
    reference: chr 17
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.328+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.328+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.170+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.793+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.793+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.227+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.199+50G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*453+50G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2437
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

17-79682677-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682677
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682677
    reference: chr 17
allele count: 26
allele frequency: 2.165042884503289e-4
allele num: 120090
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-46C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-52C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1958
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS

17-79682678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682678
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682678
    reference: chr 17
allele count: 4
allele frequency: 3.330058775537388e-5
allele num: 120118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-45G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-45G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-51G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-45G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-45G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-45G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-45G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-45G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6183
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

17-79682678-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682678
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682678
    reference: chr 17
allele count: 2
allele frequency: 1.665029387768694e-5
allele num: 120118
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-45G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-45G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-45G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-45G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-45G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-51G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-45G>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-45G>C
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42203
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-79682680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682680
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682680
    reference: chr 17
allele count: 27
allele frequency: 2.246480513861617e-4
allele num: 120188
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-43C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-43C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-43C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-43C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-49C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-43C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-43C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-43C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42204
  bin: 9.75e1
  variant carriers: 27
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

17-79682687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682687
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682687
    reference: chr 17
allele count: 11
allele frequency: 9.143351121307333e-5
allele num: 120306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-36C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-36C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-36C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-36C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-36C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-36C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-42C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-36C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6318
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42205
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD

17-79682690-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682690
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682690
    reference: chr 17
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-33C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-33C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-33C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-33C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-33C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-39C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-33C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-33C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42200
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-79682692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682692
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682692
    reference: chr 17
allele count: 9
allele frequency: 7.478188616535106e-5
allele num: 120350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-37C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-31C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-31C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42201
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

17-79682693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682693
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682693
    reference: chr 17
allele count: 6
allele frequency: 4.984051036682616e-5
allele num: 120384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-30G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-36G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42201
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

17-79682695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682695
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682695
    reference: chr 17
allele count: 17
allele frequency: 1.411866321174673e-4
allele num: 120408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-34C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-28C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-28C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-28C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-28C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-28C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-28C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-28C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42205
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 6388
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-79682700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682700
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682700
    reference: chr 17
allele count: 55
allele frequency: 4.566892520260396e-4
allele num: 120432
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-23C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-29C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-23C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42215
  bin: 9.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

17-79682716-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682716
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682716
    reference: chr 17
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-7A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-13A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-7A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-7A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-7A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-7A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-7A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-7A>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6480
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2286
  bin: 9.25e1
  variant carriers: 0
hgvs: c.794-7A>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

17-79682718-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682718
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682718
    reference: chr 17
allele count: 2
allele frequency: 1.660054117764239e-5
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-11C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-5C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-5C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-5C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-5C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-5C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-5C>G
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-5C>G
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
hgvs: c.794-5C>G
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

17-79682718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682718
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682718
    reference: chr 17
allele count: 4
allele frequency: 3.320108235528479e-5
allele num: 120478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-5C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-5C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-5C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-5C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-5C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-11C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-5C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-5C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: c.794-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

17-79682719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682719
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682719
    reference: chr 17
allele count: 5
allele frequency: 4.150066401062417e-5
allele num: 120480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-4G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-4G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-4G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-4G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-4G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-4G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-10G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-4G>A
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6464
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2288
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: c.794-4G>A
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

17-79682721-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682721
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682721
    reference: chr 17
allele count: 2
allele frequency: 1.659861235600704e-5
allele num: 120492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.200-2A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.329-2A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*454-2A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.329-2A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.171-8A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.794-2A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.228-2A>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.794-2A>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
hgvs: c.794-2A>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

17-79682731-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682731
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682731
    reference: chr 17
allele count: 3
allele frequency: 2.490908185124296e-5
allele num: 120438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.236G>A
  hgvsp: ENSP00000458785.1:p.Gly80Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.337G>A
  hgvsp: ENSP00000328403.5:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.802G>A
  hgvsp: ENSP00000461324.1:p.Gly268Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*462G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.173G>A
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.802G>A
  hgvsp: ENSP00000439565.1:p.Gly268Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.208G>A
  hgvsp: ENSP00000446242.1:p.Gly70Arg
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.337G>A
  hgvsp: ENSP00000345580.5:p.Gly113Arg
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly113Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

17-79682736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682736
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682736
    reference: chr 17
allele count: 1
allele frequency: 8.304130474498016e-6
allele num: 120422
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.342C>T
  hgvsp: ENST00000331531.5:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.241C>T
  hgvsp: ENST00000574884.1:c.241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.807C>T
  hgvsp: ENST00000541223.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.178C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.213C>T
  hgvsp: ENST00000545862.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.342C>T
  hgvsp: ENST00000350690.5:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.807C>T
  hgvsp: ENST00000571730.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*467C>T
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly114Gly
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-79682738-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682738
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682738
    reference: chr 17
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.344T>C
  hgvsp: ENSP00000345580.5:p.Phe115Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.344T>C
  hgvsp: ENSP00000328403.5:p.Phe115Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.215T>C
  hgvsp: ENSP00000446242.1:p.Phe72Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.809T>C
  hgvsp: ENSP00000439565.1:p.Phe270Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.243T>C
  hgvsp: ENSP00000458785.1:p.Phe82Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.809T>C
  hgvsp: ENSP00000461324.1:p.Phe270Ser
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.180T>C
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*469T>C
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2501
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6352
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe115Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

17-79682739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 79682739
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 79682739
    reference: chr 17
allele count: 11
allele frequency: 9.136516163327685e-5
allele num: 120396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000446242
  ensembl transcript: ENST00000545862
  gene symbol: SLC25A10
  hgvsc: ENST00000545862.1:c.216C>T
  hgvsp: ENST00000545862.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000439565
  ensembl transcript: ENST00000541223
  gene symbol: SLC25A10
  hgvsc: ENST00000541223.1:c.810C>T
  hgvsp: ENST00000541223.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183048
  ensembl transcript: ENST00000571876
  gene symbol: SLC25A10
  hgvsc: ENST00000571876.1:n.181C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000460597
  ensembl transcript: ENST00000574129
  gene symbol: SLC25A10
  hgvsc: ENST00000574129.1:c.*470C>T
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000262660
  ensembl protein: ENSP00000461324
  ensembl transcript: ENST00000571730
  gene symbol: SLC25A10
  hgvsc: ENST00000571730.1:c.810C>T
  hgvsp: ENST00000571730.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000328403
  ensembl transcript: ENST00000331531
  gene symbol: SLC25A10
  hgvsc: ENST00000331531.5:c.345C>T
  hgvsp: ENST00000331531.5:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000345580
  ensembl transcript: ENST00000350690
  gene symbol: SLC25A10
  hgvsc: ENST00000350690.5:c.345C>T
  hgvsp: ENST00000350690.5:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000183048
  ensembl protein: ENSP00000458785
  ensembl transcript: ENST00000574884
  gene symbol: SLC25A10
  hgvsc: ENST00000574884.1:c.244C>T
  hgvsp: ENST00000574884.1:c.244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10980
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe115Phe
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1099
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46213
bin: 9.75e1
variant carriers: 9

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.870091011095873e-4
allele num: 16042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64818
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.078810759792355e-4
allele num: 8476
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

DP
type: SiteQuality
SIO_000300: 5.748698e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

QD
type: SiteQuality
SIO_000300: 1.195e1

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

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46223
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64902
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.484780718101627e-4
allele num: 16098
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 3.691e0

DP
type: SiteQuality
SIO_000300: 5.753947e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.581e1

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeQuality
all individuals: 1923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46245
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 999
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533554165133113e-5
allele num: 65208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

FS
type: SiteQuality
SIO_000300: 1.404e0

QD
type: SiteQuality
SIO_000300: 1.471e1

VQSLOD
type: SiteQuality
SIO_000300: -8.09e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.268e0

DP
type: SiteQuality
SIO_000300: 5.766997e6

GenotypeQuality
all individuals: 46260
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5861
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
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: 15
allele frequency: 2.296176101399137e-4
allele num: 65326
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 6.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 5.773106e6

QD
type: SiteQuality
SIO_000300: 1.321e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73550850399167e-4
allele num: 11524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529847321237341e-5
allele num: 65366
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.236e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 5.773885e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.042e1

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46294
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045530683721638e-5
allele num: 65670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.068e1

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: -3.716e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-1

DP
type: SiteQuality
SIO_000300: 5.78229e6

GenotypeQuality
all individuals: 559
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2073
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46315
bin: 9.75e1
variant carriers: 115

GenotypeQuality
all individuals: 947
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5924
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 114
allele frequency: 1.112195121951219e-2
allele num: 10250
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.59920291110726e-4
allele num: 11542
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.98e0

DP
type: SiteQuality
SIO_000300: 5.79814e6

QD
type: SiteQuality
SIO_000300: 1.303e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.113e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1189
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2073
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46310
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041825095057034e-5
allele num: 65750
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.092e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.61e-1

FS
type: SiteQuality
SIO_000300: 1.751e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 5.797396e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46315
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519295047098146e-5
allele num: 65820
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.696e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.329e1

DP
type: SiteQuality
SIO_000300: 5.798196e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.82e0

VQSLOD
type: SiteQuality
SIO_000300: 6.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.57e-1

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46316
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5873
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variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038220817889044e-5
allele num: 65828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.066e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.345e1

DP
type: SiteQuality
SIO_000300: 5.799467e6

MQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

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

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2092
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 664
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variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.062763793155801e-4
allele num: 65866
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.800973e6

QD
type: SiteQuality
SIO_000300: 1.269e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

GenotypeQuality
all individuals: 1199
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46319
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.035546246547066e-5
allele num: 65886
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 1.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

DP
type: SiteQuality
SIO_000300: 5.801043e6

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5929
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65912
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 5.801483e6

QD
type: SiteQuality
SIO_000300: 1.08e1

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 1.114e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.194e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 474
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 44
bin: 4.25e1
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GenotypeQuality
all individuals: 665
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GenotypeQuality
all individuals: 46323
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 2118
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GenotypeQuality
all individuals: 5926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
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GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 9.25e1
variant carriers: 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: 11552
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.946282600233554e-4
allele num: 10276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.033612425676495e-5
allele num: 65928
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 5.801476e6

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.632e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.25e-1

FS
type: SiteQuality
SIO_000300: 1.094e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.15e-1

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 9.25e1
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GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 2115
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GenotypeQuality
all individuals: 46323
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
all individuals: 91
bin: 3.25e1
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 666
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GenotypeQuality
all individuals: 61
bin: 5.25e1
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GenotypeQuality
all individuals: 5930
bin: 6.25e1
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GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.549452549209912e-5
allele num: 65942
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.03e-1

QD
type: SiteQuality
SIO_000300: 1.269e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.58e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

DP
type: SiteQuality
SIO_000300: 5.802829e6

GenotypeQuality
all individuals: 52156
bin: 9.75e1
variant carriers: 37907

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 16

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 20

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1172
bin: 6.75e1
variant carriers: 45

GenotypeQuality
all individuals: 501
bin: 8.75e1
variant carriers: 42

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 40

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 13

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 30

GenotypeQuality
all individuals: 3162
bin: 6.25e1
variant carriers: 42

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 876
bin: 9.25e1
variant carriers: 42

GenotypeQuality
all individuals: 822
bin: 8.25e1
variant carriers: 38

African
type: Population
allele count: 5049
allele frequency: 4.884868421052632e-1
allele num: 10336
num of homozygotes: 1248

European (Non-Finnish)
type: Population
allele count: 26153
allele frequency: 3.952275887082149e-1
allele num: 66172
num of homozygotes: 5175

South Asian
type: Population
allele count: 5517
allele frequency: 3.341611144760751e-1
allele num: 16510
num of homozygotes: 957

Latino
type: Population
allele count: 5502
allele frequency: 4.758692267773741e-1
allele num: 11562
num of homozygotes: 1304

European (Finnish)
type: Population
allele count: 2350
allele frequency: 3.553069247051708e-1
allele num: 6614
num of homozygotes: 427

Other
type: Population
allele count: 349
allele frequency: 3.88641425389755e-1
allele num: 898
num of homozygotes: 77

East Asian
type: Population
allele count: 3132
allele frequency: 3.65120074609466e-1
allele num: 8578
num of homozygotes: 571

DP
type: SiteQuality
SIO_000300: 1.0956018e7

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.59e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

QD
type: SiteQuality
SIO_000300: 1.759e1

GenotypeQuality
all individuals: 1692
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 490
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66060
num of homozygotes: 0

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

African
type: Population
allele count: 16
allele frequency: 1.551590380139643e-3
allele num: 10312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.541e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

DP
type: SiteQuality
SIO_000300: 4.359318e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.214e0

GenotypeQuality
all individuals: 2267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44309
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514050387596899e-5
allele num: 66048
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 2.522e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.979e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 4.355912e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.25e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

GenotypeQuality
all individuals: 554
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44308
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

QD
type: SiteQuality
SIO_000300: 9.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.491e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 4.355152e6

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

GenotypeQuality
all individuals: 1651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5613
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1070
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44307
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514233797698365e-5
allele num: 66040
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.885003885003885e-4
allele num: 10296
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

DP
type: SiteQuality
SIO_000300: 4.354754e6

FS
type: SiteQuality
SIO_000300: 2.726e0

QD
type: SiteQuality
SIO_000300: 1.253e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 1945
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44305
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1039
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.57346258709482e-5
allele num: 66020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058361052313275e-3
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

MQ
type: SiteQuality
SIO_000300: 6.039e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 4.353818e6

VQSLOD
type: SiteQuality
SIO_000300: 3.73e0

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

QD
type: SiteQuality
SIO_000300: 1.469e1

FS
type: SiteQuality
SIO_000300: 1.228e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 594
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44292
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65964
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

QD
type: SiteQuality
SIO_000300: 2.162e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.069e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

DP
type: SiteQuality
SIO_000300: 4.351239e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5566
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: 2
allele frequency: 3.031589159037167e-5
allele num: 65972
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

MQ
type: SiteQuality
SIO_000300: 5.868e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.191e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.13e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 4.352989e6

GenotypeQuality
all individuals: 1678
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44296
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1943
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517174414370676e-5
allele num: 65912
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 11556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.349272e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.004e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.954000000000001e0

QD
type: SiteQuality
SIO_000300: 1.284e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 8.25e1
variant carriers: 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: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.488372093023256e-4
allele num: 8600
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

QD
type: SiteQuality
SIO_000300: 1.501e1

VQSLOD
type: SiteQuality
SIO_000300: 8.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.348277e6

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65890
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.262e0

DP
type: SiteQuality
SIO_000300: 4.347196e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.687e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeQuality
all individuals: 876
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 1044
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variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.089021494245874e-5
allele num: 65692
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.123e0

MQRankSum
type: SiteQuality
SIO_000300: 9.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 4.339591e6

QD
type: SiteQuality
SIO_000300: 1.462e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.68e-1

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 179
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65674
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

DP
type: SiteQuality
SIO_000300: 4.338922e6

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 8

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.090690379754545e-5
allele num: 65674
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.813542688910697e-5
allele num: 10190
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.328e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

MQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 4.338922e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.964250638381458e-4
allele num: 10182
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.216e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

DP
type: SiteQuality
SIO_000300: 4.337704e6

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

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: 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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bin: 4.25e1
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GenotypeQuality
all individuals: 1034
bin: 8.75e1
variant carriers: 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: 10156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525506468147425e-5
allele num: 65552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.116e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.914e0

DP
type: SiteQuality
SIO_000300: 4.33468e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 1936
bin: 9.25e1
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GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.34796900680911e-4
allele num: 8518
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530596626565035e-5
allele num: 65334
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.962e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.452e1

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 4.327656e6

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 102
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44278
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.684997395913115e-4
allele num: 65282
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

FS
type: SiteQuality
SIO_000300: 3.401e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 1.572e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

DP
type: SiteQuality
SIO_000300: 4.326398e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.155e0

GenotypeQuality
all individuals: 382
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1937
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65338
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
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: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.325073e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.563e0

FS
type: SiteQuality
SIO_000300: 1.362e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 1.479e1

GenotypeQuality
all individuals: 1651
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 9.25e1
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GenotypeQuality
all individuals: 4504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44268
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1633
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

DP
type: SiteQuality
SIO_000300: 4.325277e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

FS
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.13e-1

GenotypeQuality
all individuals: 1633
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1651
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532285250222181e-5
allele num: 65262
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.325277e6

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 1.276e1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

FS
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

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

GenotypeQuality
all individuals: 1971
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44278
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 239
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532332209623046e-5
allele num: 65260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.536e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 4.324223e6

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532379171902295e-5
allele num: 65258
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 1.111e0

MQRankSum
type: SiteQuality
SIO_000300: -1.029e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.086e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.416e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

QD
type: SiteQuality
SIO_000300: 1.194e1

DP
type: SiteQuality
SIO_000300: 4.324783e6

GenotypeQuality
all individuals: 1632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4704
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1936
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variant carriers: 0

GenotypeQuality
all individuals: 44273
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.080505898090721e-5
allele num: 16446
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.591789879695105e-5
allele num: 65334
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 1.115e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.395e1

DP
type: SiteQuality
SIO_000300: 4.325417e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

GenotypeQuality
all individuals: 193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4693
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1033
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.00060036021613e-4
allele num: 9994
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.215e0

VQSLOD
type: SiteQuality
SIO_000300: -2.551e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.165e0

DP
type: SiteQuality
SIO_000300: 4.324738e6

FS
type: SiteQuality
SIO_000300: 2.996e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 2.115e1

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44281
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1671
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
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: 11494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.216693028348948e-4
allele num: 16438
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65374
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 2.984e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.325811e6

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 990
bin: 8.75e1
variant carriers: 14

GenotypeQuality
all individuals: 286
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 170
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4471
bin: 6.25e1
variant carriers: 12

GenotypeQuality
all individuals: 1562
bin: 8.25e1
variant carriers: 10

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1858
bin: 9.25e1
variant carriers: 15

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 45447
bin: 9.75e1
variant carriers: 13061

European (Non-Finnish)
type: Population
allele count: 8959
allele frequency: 1.368789341807737e-1
allele num: 65452
num of homozygotes: 613

European (Finnish)
type: Population
allele count: 1080
allele frequency: 1.637355973317162e-1
allele num: 6596
num of homozygotes: 89

East Asian
type: Population
allele count: 4
allele frequency: 4.71253534401508e-4
allele num: 8488
num of homozygotes: 0

South Asian
type: Population
allele count: 1249
allele frequency: 7.597323600973235e-2
allele num: 16440
num of homozygotes: 64

Latino
type: Population
allele count: 766
allele frequency: 6.668988333623542e-2
allele num: 11486
num of homozygotes: 32

African
type: Population
allele count: 1987
allele frequency: 1.979477983662084e-1
allele num: 10038
num of homozygotes: 199

Other
type: Population
allele count: 103
allele frequency: 1.157303370786517e-1
allele num: 890
num of homozygotes: 7

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

FS
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.188e0

QD
type: SiteQuality
SIO_000300: 1.59e1

DP
type: SiteQuality
SIO_000300: 4.32215e6

GenotypeQuality
all individuals: 2290
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17813383600377e-4
allele num: 8488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65404
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.738e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: -3.427e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 1.5412e1

DP
type: SiteQuality
SIO_000300: 3.212585e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.18e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42214
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1202
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65430
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.713e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

VQSLOD
type: SiteQuality
SIO_000300: -4.02e0

DP
type: SiteQuality
SIO_000300: 3.212719e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.968e0

MQ
type: SiteQuality
SIO_000300: 5.226e1

FS
type: SiteQuality
SIO_000300: 2.0902e1

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42214
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1936
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.216249087813184e-4
allele num: 16444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52895847348786e-5
allele num: 65404
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.968102073365231e-5
allele num: 10032
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 3.212944e6

VQSLOD
type: SiteQuality
SIO_000300: -1.748e0

QD
type: SiteQuality
SIO_000300: 2.756e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.446e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42215
bin: 9.75e1
variant carriers: 24

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 1.89017111022682e-3
allele num: 10052
num of homozygotes: 1

Latino
type: Population
allele count: 3
allele frequency: 2.610057421263268e-4
allele num: 11494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053714844107857e-5
allele num: 65494
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

FS
type: SiteQuality
SIO_000300: 1.091e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

DP
type: SiteQuality
SIO_000300: 3.21465e6

QD
type: SiteQuality
SIO_000300: 1.658e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5672
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 212
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

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

African
type: Population
allele count: 7
allele frequency: 6.927949326999208e-4
allele num: 10104
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.214384e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.84e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.252e1

MQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

GenotypeQuality
all individuals: 174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 1933
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variant carriers: 0

GenotypeQuality
all individuals: 42201
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variant carriers: 1

GenotypeQuality
all individuals: 1244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524483200195134e-5
allele num: 65596
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

QD
type: SiteQuality
SIO_000300: 1.466e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

FS
type: SiteQuality
SIO_000300: 4.289e0

VQSLOD
type: SiteQuality
SIO_000300: 5.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.01e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 3.21484e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

GenotypeQuality
all individuals: 165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1226
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2398
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175088131609871e-4
allele num: 8510
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 42
allele frequency: 2.55133033653262e-3
allele num: 16462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.8833761612967e-5
allele num: 10118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.332602005058354e-4
allele num: 65634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.064281382656155e-4
allele num: 6596
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.32e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.681e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.342e1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 3.217697e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
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GenotypeQuality
all individuals: 55
bin: 5.75e1
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GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
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GenotypeQuality
all individuals: 2404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
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variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.569826955885937e-5
allele num: 65648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.877518767285657e-5
allele num: 10124
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 3.21224e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e0

QD
type: SiteQuality
SIO_000300: 1.383e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.125e0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1950
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
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GenotypeQuality
all individuals: 1226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.75e1
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GenotypeQuality
all individuals: 42199
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3609e1

VQSLOD
type: SiteQuality
SIO_000300: -2.145e0

DP
type: SiteQuality
SIO_000300: 3.212456e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.653e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: -4.44e-1

QD
type: SiteQuality
SIO_000300: 1.377e1

GenotypeQuality
all individuals: 1950
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42197
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 650
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1959
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521236460995497e-5
allele num: 65736
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: 16474
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

FS
type: SiteQuality
SIO_000300: 6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.42e0

QD
type: SiteQuality
SIO_000300: 2.648e1

DP
type: SiteQuality
SIO_000300: 3.214653e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.86e-1

GenotypeQuality
all individuals: 42209
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 6131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.941176470588235e-4
allele num: 10200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.73572861572132e-4
allele num: 65796
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.426301103967002e-4
allele num: 16486
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.275e0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

DP
type: SiteQuality
SIO_000300: 3.216942e6

FS
type: SiteQuality
SIO_000300: 1.773e0

GenotypeQuality
all individuals: 1239
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42203
bin: 9.75e1
variant carriers: 4

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

South Asian
type: Population
allele count: 3
allele frequency: 1.819505094614265e-4
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 1
allele frequency: 1.519433555170632e-5
allele num: 65814
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.37e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.22e-1

FS
type: SiteQuality
SIO_000300: 2.524e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 3.21648e6

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.038867110341265e-5
allele num: 65814
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 2.524e0

DP
type: SiteQuality
SIO_000300: 3.21648e6

QD
type: SiteQuality
SIO_000300: 1.37e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.22e-1

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 27
allele frequency: 2.338472198163866e-3
allele num: 11546
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.439e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.383e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

DP
type: SiteQuality
SIO_000300: 3.217791e6

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

GenotypeQuality
all individuals: 1963
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65910
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 11
allele frequency: 1.072333788262819e-3
allele num: 10258
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: -5.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.15e-1

DP
type: SiteQuality
SIO_000300: 3.216438e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.411e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.315e1

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

GenotypeQuality
all individuals: 1251
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 6336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516806212838248e-5
allele num: 65928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.215983e6

QD
type: SiteQuality
SIO_000300: 1.389e1

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 2498
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6351
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.424536307431204e-4
allele num: 16498
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.919423900350331e-4
allele num: 10276
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516760200212346e-5
allele num: 65930
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.168e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 3.216523e6

FS
type: SiteQuality
SIO_000300: 1.737e0

VQSLOD
type: SiteQuality
SIO_000300: 9.65e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

GenotypeQuality
all individuals: 1253
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.064649160046092e-5
allele num: 65956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
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: 10278
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.216262e6

MQRankSum
type: SiteQuality
SIO_000300: 8.02e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

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

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 4.860976083997667e-4
allele num: 10286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 65966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.273608922293612e-4
allele num: 16498
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

QD
type: SiteQuality
SIO_000300: 1.238e1

FS
type: SiteQuality
SIO_000300: 4.112e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 3.216772e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.553e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-1

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

GenotypeQuality
all individuals: 6440
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 480
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

African
type: Population
allele count: 54
allele frequency: 5.244755244755245e-3
allele num: 10296
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

QD
type: SiteQuality
SIO_000300: 1.301e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.138e0

DP
type: SiteQuality
SIO_000300: 3.218551e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42196
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1975
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515105602860519e-5
allele num: 66002
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 3.213886e6

FS
type: SiteQuality
SIO_000300: 5.254e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.368e0

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.348e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 1973
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42196
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029935765361774e-5
allele num: 66008
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 3.214081e6

VQSLOD
type: SiteQuality
SIO_000300: -1.121e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.417e0

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 1.108e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42196
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 484
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.059871530723549e-5
allele num: 66008
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
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: 8620
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.182e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.417e0

VQSLOD
type: SiteQuality
SIO_000300: -1.121e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

FS
type: SiteQuality
SIO_000300: 1.108e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 3.214081e6

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42195
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.030670384289005e-4
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66006
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.278e0

QD
type: SiteQuality
SIO_000300: 1.134e1

DP
type: SiteQuality
SIO_000300: 3.213236e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.241e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1974
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42193
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6480
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.942879347192539e-4
allele num: 10294
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

QD
type: SiteQuality
SIO_000300: 1.125e1

DP
type: SiteQuality
SIO_000300: 3.212762e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42193
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.547659471258792e-5
allele num: 65968
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.066e0

DP
type: SiteQuality
SIO_000300: 3.211643e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.752e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.153e1

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 516
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2505
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2290
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

European (Finnish)
type: Population
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: 8620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515932450050026e-5
allele num: 65966
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

DP
type: SiteQuality
SIO_000300: 3.210865e6

FS
type: SiteQuality
SIO_000300: 7.315e0

QD
type: SiteQuality
SIO_000300: 1.164e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.936e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42192
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 1
allele frequency: 1.516070345664039e-5
allele num: 65960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.876e1

QD
type: SiteQuality
SIO_000300: 1.113e1

FS
type: SiteQuality
SIO_000300: 3.431e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.549e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

DP
type: SiteQuality
SIO_000300: 3.210428e6